Inflatable bariatric clamp

ABSTRACT

A bariatric clamp may include substrate members overmolded in polymer forming first and second elongated portions, a bight portion having a flexible hinge, one or more inflatable portions disposed at least partially along interior sections of the first and second elongated portions; and a port coupled to at least one of the inflatable portions and configured to adjust inflation of the inflatable portions. The inflatable portions are provided to assist in retaining the clamp in a closed position to partition the stomach and to adjust a pressure of the clamp when partitioning the stomach.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims priority to, and the benefit of, U.S.Provisional Patent Application Ser. No. 62/359,529 entitled “INFLATABLEBARIATRIC CLAMP” filed on Jul. 7, 2016, the contents of which are herebyincorporated herein by reference in their entirety for any purpose.

FIELD

The present disclosure relates generally to surgical clamps and surgicalclamp installation tools.

BACKGROUND

The statements in this section merely provide background informationrelated to the present disclosure and may not constitute prior art.

Recently, there has been increased interest in employing surgical clampsto partition sections of a stomach. An example of a bariatric surgicalclamp can be found in Jacobs et al., U.S. patent application Ser. No.11/984,452, Jacobs et al., U.S. patent application Ser. No. 11/797,537and Jacobs et al. U.S. patent application Ser. No. 13/017,666. Theaforementioned patent applications are incorporated by reference hereinin their entirety for any purpose.

SUMMARY

In one embodiment, the present disclosure provides a bariatric clampcomprising: a first elongated portion having a distal end, a proximalend, and a first polymer portion; a second elongated portion having adistal end, a proximal end, and a second polymer portion; a bightportion having a flexible hinge formed at least partially from a thirdpolymer portion, the bight portion joining the first and secondelongated portions at the proximal end of the first elongated portion ofthe bariatric clamp and the proximal end of the second elongated portionof the bariatric clamp; an inflatable portion disposed at leastpartially along an interior section of the first elongated portion ofthe bariatric clamp; and a port coupled to the inflatable portion andconfigured to adjust inflation of the inflatable portion.

In another embodiment, the present disclosure provides a bariatric clampinstallation system, comprising: a bariatric clamp, the bariatric clampincluding: a first elongated portion having a distal end, a proximalend, and a first polymer portion, a second elongated portion having adistal end, a proximal end, and a second polymer portion, a bightportion having a flexible hinge formed at least partially from a thirdpolymer portion, the bight portion joining the first and secondelongated portions at the proximal end of the first elongated portion ofthe bariatric clamp and the proximal end of the second elongated portionof the bariatric clamp, a first inflatable portion disposed at leastpartially along an interior section of the first elongated portion, asecond inflatable portion disposed at least partially along an interiorsection of the second elongated portion, and a port coupled to at leastone of the first and second inflatable portions and configured to adjustinflation of at least one of the first and second inflatable portions;and a bariatric clamp installation tool, the bariatric clampinstallation tool including: an elongated member having a chamberextending from a proximal end of the elongated member to a distal end ofthe elongated member, the elongated member configured to retain thebariatric clamp in an open position along a length of the elongatedmember, a cable member having a proximal end and a distal end, the cablemember extending along a length of the chamber of the elongated member,a handle positioned adjacent the proximal end of the elongated memberand attached to the proximal end of the cable member, wherein the handleis configured to engage the cable member, and an articulating headlocated at the distal end of the elongated member and attached to thedistal end of the cable member, wherein the articulating head isconfigured to articulate a portion of the bariatric clamp in response tothe handle engaging the cable member.

Further embodiments and apparatuses, including other areas ofapplicability, will become apparent from the description providedherein. It should be understood that the description and specificexamples are intended for purposes of illustration only and are notintended to limit the scope of the present disclosure in any manner.

BRIEF DESCRIPTION OF THE DRAWINGS

For a more complete understanding of various embodiments of the presentinvention and the advantages thereof, reference is now made to thefollowing brief description, taken in connection with the accompanyingdrawings and detailed description, wherein like reference numeralsrepresent like parts, and in which:

FIG. 1 is a view of an embodiment of a surgical clamp engaged with anembodiment of a surgical clamp installation tool having an articulatinghead;

FIGS. 2(a)-2(c) illustrate engagement of the surgical clamp to thearticulating head of the surgical clamp installation tool;

FIG. 2(d) illustrates the surgical clamp in an open position;

FIG. 2(e) illustrates the surgical clamp after actuation to a closedposition;

FIG. 2(f) illustrates a top view of the surgical clamp;

FIG. 2(g) illustrates a left side view of the surgical clamp;

FIG. 2(h) illustrates a bottom view of the surgical clamp;

FIG. 2(i) illustrates a right side view of the surgical clamp;

FIG. 2(j) illustrates a view facing the distal end of the surgical clamp

FIG. 2(k) illustrates a view facing the proximal end of the surgicalclamp;

FIG. 3(a) is a left side view of the surgical clamp installation tool;

FIG. 3(b) is a top view of the surgical clamp installation tool;

FIG. 3(c) a right side view of the surgical clamp installation tool withthe right side of the housing of the handle shown removed;

FIG. 3(d) is a bottom view of the surgical clamp installation tool;

FIG. 3(e) is a view facing the distal end of the surgical clampinstallation tool;

FIG. 3(f) is a view facing the proximal end of the surgical clampinstallation tool;

FIG. 4(a) is a perspective view illustrating an exemplary surgical clampinstallation tool with the right side of the housing of the handle shownremoved;

FIGS. 4(b), 4(c), 4(d), and 4(e) provide side cutaway views of variousaspects of an embodiment of the surgical clamp installation tool;

FIG. 5 is a view of another embodiment of a surgical clamp engaged withanother embodiment of a surgical clamp installation tool having anarticulating head;

FIG. 6A is a top view of a rigid member having a male clasp end for theclamp of FIG. 5;

FIG. 6B is a side view of the rigid member of FIG. 6A having the maleclasp end for the clamp of FIG. 5;

FIG. 6C is a side view showing the male clasp end of FIG. 6B in greaterdetail;

FIG. 6D is a cross-sectional view showing a cross-section of the rigidmember of FIG. 6A;

FIG. 7A is a top view of a rigid member having a female clasp end forthe clamp of FIG. 5;

FIG. 7B is a side view of the rigid member of FIG. 7A having the femaleclasp end for the clamp of FIG. 5;

FIG. 7C is a side view showing the female clasp end of FIG. 7B ingreater detail;

FIG. 7D is a cross-sectional view showing a cross-section of the rigidmember of FIG. 7A;

FIG. 8A is a top view of a spring member for the clamp of FIG. 5;

FIG. 8B is a side view of the spring member for the clamp of FIG. 5;

FIG. 8C is a cross-sectional, close-up view showing a cross-section ofthe spring member of FIG. 8B;

FIG. 8D is a proximal end view of the spring member of FIG. 5;

FIG. 9A is a side view of the clamp of FIG. 5;

FIG. 9B is a bottom view of the clamp of FIG. 5;

FIG. 9C is a proximal end view of the clamp of FIG. 5;

FIG. 9D is a perspective view of the clamp of FIG. 5;

FIG. 10 is a view illustrating the surgical clamp installed in asubstantially vertical position on a human stomach;

FIG. 11 is a flow diagram illustrating an embodiment of a method forclamping an internal organ;

FIG. 12 is a flow diagram illustrating another embodiment of a methodfor clamping an internal organ;

FIG. 13 is a view of yet another embodiment of a surgical clamp engagedwith yet another embodiment of a surgical clamp installation tool havingan articulating head;

FIG. 14 is a perspective view of the surgical clamp of FIG. 13;

FIG. 15(a) is a top view of the surgical clamp of FIG. 14;

FIG. 15(b) is a left view of the surgical clamp of FIG. 14;

FIG. 15(c) is a bottom view of the surgical clamp of FIG. 14;

FIG. 15(d) is a right view of the surgical clamp of FIG. 14;

FIG. 15(e) is a proximal spring end on view of the surgical clamp ofFIG. 14;

FIG. 15(f) is a distal latch end on view of the surgical clamp of FIG.14;

FIG. 16 is a detailed view of a latch end of a bottom arm of thesurgical clamp of FIG. 14;

FIG. 17(a) is a top view of the surgical clamp installation tool of FIG.13;

FIG. 17(b) is a left view of the surgical clamp installation tool ofFIG. 13;

FIG. 17(c) is a bottom view of the surgical clamp installation tool ofFIG. 13;

FIG. 17(d) is a right view of the surgical clamp installation tool ofFIG. 13;

FIG. 17(e) is a proximal handle end on view of the surgical clampinstallation tool of FIG. 13;

FIG. 17(f) is a distal head end on view of the surgical clampinstallation tool of FIG. 13;

FIG. 18 is a detailed left side view of a handle end of the surgicalclamp installation tool FIG. 13 in which the left side of the handlehousing is shown removed;

FIG. 19 is a perspective view of the surgical clamp of FIG. 14 having asilicone sleeve engaged therewith;

FIG. 20 is a perspective view of the silicone sleeve of FIG. 19 in adisengaged state;

FIG. 21 is a bottom view of the silicone sleeve of FIG. 20;

FIG. 22 is a proximal end-on view of the silicone sleeve of FIG. 20;

FIG. 23 is a top view of the silicone sleeve of FIG. 20;

FIG. 24 is a left side view of the silicone sleeve of FIG. 20;

FIG. 25 is a cross-sectional view of a distal end of the silicone sleeveof FIG. 23;

FIG. 26 is a cross-sectional view of a proximal end of the siliconesleeve of FIG. 24;

FIG. 27 is a cross sectional view of a proximal end of FIG. 23;

FIG. 28 is a flow diagram illustrating a method of performing endoscopicsurgery utilizing the silicone sleeve, clamp, and installation tool ofFIGS. 13-27;

FIG. 29 is a perspective view of an embodiment of a one-piece surgicalclamp comprised of first and second substrate members overmolded in apolymer material;

FIGS. 30(a) and 30(b) illustrate respective side and perspective viewsof the one-piece surgical clamp of FIG. 29, wherein the polymer materialis illustrated semitransparent to show the first and second substratemembers;

FIGS. 31(a) and 31(b) illustrate the respective first and secondsubstrate members of the one-piece surgical clamp of FIG. 29;

FIG. 32 illustrates another embodiment of a one-piece surgical clampcomprised of first and second substrate members overmolded in a polymermaterial;

FIG. 33 is a perspective view of an embodiment of an installation toolused to install a one-piece surgical clamp;

FIGS. 34(a), 34(b) and 34(c) illustrate various views of yet anotherembodiment of a one-piece surgical clamp comprised of first and secondsubstrate members overmolded in a polymer material;

FIG. 35 is a perspective view of yet another embodiment of a one-piecesurgical clamp comprised of first and second substrate membersovermolded in a polymer material;

FIG. 36 is a flow diagram illustrating an embodiment of a method forclamping an internal organ;

FIG. 37 is a flow diagram illustrating another embodiment of a methodfor clamping an internal organ;

FIG. 38 is a perspective view of an embodiment of a two-piece surgicalclamp comprised of first and second substrate members, each overmoldedin a polymer material;

FIGS. 39(a), 39(b) and 39(c) illustrate various views of the two-piecesurgical clamp of FIG. 38;

FIG. 40 is a perspective view of another embodiment of a two-piecesurgical clamp comprised of first and second substrate members, eachovermolded in a polymer material;

FIGS. 41(a)-41(e) illustrate various views of an embodiment of abariatric clamp;

FIGS. 42(a) and 42(b) illustrate an embodiment of an adjustablebariatric clamp in a retracted position and an extended position,respectively;

FIGS. 43(a) and 43(b) illustrate an embodiment of an adjustablebariatric clamp in a retracted position and an extended position,respectively;

FIGS. 44(a) and 44(b) illustrate an embodiment of an adjustablebariatric clamp having a ratchet feature, wherein the clamp is shown ina retracted position and an extended position, respectively;

FIG. 45 is a flow diagram illustrating a method of installing abariatric clamp;

FIG. 46 illustrates the bariatric clamp of FIGS. 41(a)-41(e) in asubstantially expanded position;

FIG. 47 is a flow diagram illustrating a method of inserting a bariatricclamp into the abdominal cavity of the patient;

FIGS. 48(a) and 48(b) illustrate various views of a patient's stomach;

FIGS. 49(a) and 49(b) illustrate various views of an example embodimentof an alignment device;

FIGS. 50(a), 50(b), 50(c) and 50(d) illustrate an embodiment of thedisclosed bariatric clamp in various closed and opened positions;

FIGS. 51(a), 51(b) and 51(c) illustrate an embodiment of the disclosedbariatric clamp in various contorted positions;

FIG. 52(a) illustrates an embodiment of the disclosed clamp in a closedposition, wherein the flexible hinge is in a compressed, or non-expandedposition;

FIG. 52(b) illustrates an embodiment of the disclosed clamp in theclosed position wherein the flexible hinge is stretched or expanded;

FIGS. 53(a)-53(e) illustrate various views of the engagement feature andfastener portion of an embodiment of the disclosed bariatric clamp;

FIG. 54(a) illustrates an embodiment wherein an embodiment of thedisclosed bariatric clamp is installed on a stomach and first and secondadjustable portions are hinged such that the bight portion is angled ina first direction relative to the first and second elongated portions;

FIG. 54(b) illustrates another embodiment wherein an embodiment of thedisclosed bariatric clamp is installed on a stomach and first and secondadjustable portions are hinged such that the bight portion is angled ina second direction relative to the first and second elongated portions;

FIG. 55 illustrates an embodiment of the disclosed clamp having suturingneedles embedded in the polymer overmolding;

FIGS. 56(a) and 56(b) illustrate various views of an embodiment of theclamp having a single insert along each elongated portion;

FIGS. 56(c) and 56(d) illustrate various views of an embodiment of theclamp having a plurality of inserts along each elongated portion;

FIGS. 57(a)-57(c) illustrate various embodiments of the clamp having theinserts positioned in different locations within the elongated portionsof the clamp;

FIGS. 58(a) and 58(b) illustrate various views of an embodiment of theclamp having a single insert along each elongated portion and having nofastener or engagement portions;

FIGS. 58(c) and 58(d) illustrate various views of an embodiment of theclamp having a plurality of inserts along each elongated portion andhaving no fastener or engagement portions;

FIGS. 59(a) and 59(b) illustrate various views of an embodiment of theclamp having curved elongated portions;

FIG. 60(a) illustrates a perspective view of a patient's stomach;

FIG. 60(b) illustrates a cross section view of the stomach shown in FIG.60(a);

FIG. 61 illustrates the embodiment of the clamp having curved elongatedportions as installed on a patient's stomach;

FIG. 62 illustrates an example embodiment of a clamp;

FIGS. 63(a)-63(n) illustrate various embodiments of cross-sectionalviews of an elongated portion of the clamp illustrated in FIG. 62;

FIG. 64 illustrates an example embodiment of a polymer overmoldedbariatric clamp with suture portions;

FIG. 65 illustrates a perspective view of the clamp of FIG. 64, whereinthe polymer material is illustrated semitransparent to show the firstand second substrate members;

FIGS. 66(a) and 66(b) illustrate example embodiments of the respectivefirst and second substrate members of the clamp of FIG. 64;

FIGS. 67(a), 67(b), and 67(c) illustrate various views of an embodimentof the clamp of FIG. 64 with a portion of the overmolding removed toshow a portion of the underlying substrate;

FIG. 68 illustrates a view of the first elongated portion of the polymerovermolded bariatric clamp of FIG. 64;

FIG. 69 illustrates a view of the second elongated portion of thepolymer overmolded bariatric clamp of FIG. 64 having a portion of thepolymer overmolding removed to show the underlying substrate member;

FIG. 70 illustrates an example embodiment of a polymer overmoldedbariatric clamp having an opening in the flexible hinge of the bightportion of the clamp;

FIG. 71 illustrates an embodiment of the clamp of FIG. 70, wherein theflexible hinge includes substrate members;

FIG. 72 illustrates an embodiment of the clamp of FIG. 70, wherein theflexible hinge includes substrate members positioned in an overlappingposition;

FIG. 73 illustrates the flexible hinge of FIG. 72 in a stretchedposition wherein the substrate members encompass the opening of theflexible hinge;

FIG. 74 illustrates an example embodiment of the clamp of FIG. 70,wherein the flexible hinge includes a wired member;

FIG. 75 illustrates an embodiment of the wired member having a ringportion embedded within the overmolding of the flexible hinge andpositioned around the circumference of the opening;

FIG. 76 illustrates an embodiment of the wired member having a ringportion positioned outside of the overmolding and within the perimeterof the opening;

FIG. 77 illustrates an example embodiment of the clamp of FIG. 74 in arelaxed position wherein the wired member has extra slack embeddedwithin the flexible hinge;

FIG. 78 illustrates the clamp of FIG. 77 in a stretched position whereinthe slack of the wired member is utilized to allow the flexible hinge tostretch;

FIG. 79 illustrates an example embodiment of the clamp of FIG. 70wherein the flexible hinge includes an eyelet;

FIGS. 80(a) and 80(b) illustrate an example embodiment of the clamp ofFIG. 70 having a plate installed over the bight portion of the clamp;

FIG. 81 illustrates an example embodiment of a clamp having a T-fastenerembedded within the flexible hinge for affixing the clamp to thestomach;

FIG. 82 illustrates an example embodiment of a clamp having a looppre-attached to a suture portion for facilitating quick and easy sutureof the clamp to the stomach;

FIG. 83 illustrates an example embodiment of a clamp having a barbedsuture string with a hook at a distal end thereof for facilitating quickand easy suture of the clamp to the stomach;

FIG. 84 illustrates an example embodiment of a clamp having a suturestring with a T-shaped fastener at a distal end thereof for facilitatingquick and easy suture and anchoring of the clamp to the stomach;

FIGS. 85(a) and 85(b) illustrate an embodiment of a clamp havinginflatable portions for retaining the clamp in a substantially closedposition;

FIG. 86 illustrates an embodiment of the clamp having inflatableportions, wherein the inflatable portions are positioned within thepolymer overmolding and within recesses of the substrate members, andhaving a port positioned on each of the elongated portions of the clamp;

FIG. 87 illustrates an embodiment of the clamp having inflatableportions, wherein the inflatable portions are positioned betweensurfaces of the substrate members and the interior surface of thepolymer overmolding, and having a port positioned at the flexible hingeportion of the clamp;

FIG. 88 illustrates an embodiment of the clamp having inflatableportions, wherein the inflatable portions are positioned on an interiorsurface of the polymer overmolding, and having a port positioned on eachof the elongated portions of the clamp;

FIG. 89 illustrates an embodiment of the clamp having inflatableportions, wherein the clamp is installed on a patient's stomach andhaving a subcutaneous port for adjusting the pressure of the inflatableportions from outside the patient's body;

FIG. 90 illustrates an embodiment of the clamp having inflatableportions, wherein the inflatable portions are shown in an inflatedstate;

FIG. 91 illustrates an example embodiment of a clamp having inflatableportions and suture portions, wherein the inflatable portions are shownin an inflated state;

FIG. 92 illustrates an example embodiment of a clamp having inflatablesubstrate members;

FIG. 93 illustrates another example embodiment of a clamp havinginflatable substrate members;

FIG. 94 illustrates an example embodiment of a clamp having sets ofinflatable substrate members;

FIG. 95(a) illustrates an example embodiment of the disclosed bariatricclamp having inflatable substrate members, wherein the clamp isinstalled on a stomach and first and second adjustable portions arehinged such that the bight portion is angled in a first directionrelative to the first and second elongated portions;

FIG. 95(b) illustrates another example embodiment of the disclosedbariatric clamp having inflatable substrate members, wherein the clampis installed on a stomach and first and second adjustable portions arehinged such that the bight portion is angled in a second directionrelative to the first and second elongated portions; and

FIG. 96 illustrates another example embodiment of a bariatric clampaccording to the various example embodiments discussed herein andfurther having a tip string configured to aid installation of thebariatric clamp.

In some figures, dimensions are given in inches. However, it should beunderstood that various embodiments are not limited to the dimensionsprovided. Such dimensions are purely illustrative.

In some figures, broken lines indicate variability in length of thediscontinuous portions.

DETAILED DESCRIPTION OF THE DRAWINGS

The following description is merely exemplary in nature and is notintended to limit the present disclosure, application, or uses. Itshould be understood at the outset that although an exemplaryimplementation of the present invention is illustrated below, thepresent invention may be implemented using any number of techniques,whether currently known or in existence. The present invention should inno way be limited to the exemplary implementations, drawings, andtechniques illustrated below, including the exemplary design andimplementations illustrated and described herein. Additionally, thedrawings contained herein are not necessarily drawn to scale, and may beprovided in a variety of different dimensions, shapes andconfigurations. Any provided dimensions are provided only to illustratea particular exemplary implementation, and should in no way be construedto limit the present invention absent an explicit recitation of suchdimensions and then only with respect to the aspect or aspects recitingthe dimension or dimensions.

Referring to FIG. 1, an embodiment of a surgical clamp 100 (alsoreferred to herein as a bariatric clamp) engages with an embodiment of asurgical clamp installation tool 102. In these embodiments, the clamp100 and the installation tool 102 are designed for performing bariatricsurgery through a surgical trocar. The clamp 100, in a preferredembodiment, may be approximately fifteen to thirty centimeters in lengthto accommodate partitioning of a human stomach. To accommodate insertionthrough a trocar, the closed clamp 100 will preferably have a diameteror circumference less than fifteen millimeters over the entirety of itslength or along the majority of its length. A non-handle section of theinstallation tool 102 intended for insertion through the trocar has asimilar diameter or a smaller diameter. It is envisioned that otherembodiments of the clamp and installation tool can be of other sizes. Itis additionally envisioned that the clamp may be articulated in at leastone plane to provide different angles and lengths of partition to thestomach. It is also envisioned that other embodiments of the clamp andinstallation tool can be used for clamping other parts of the human bodyand/or for clamping other types of bodies or structures. Finally, itshould be understood that the installation tool 102 may be used toinstall embodiments of the surgical clamp other than those explicitlyillustrated in the figures.

Referring to FIG. 2(a), the surgical clamp 100 has two elongated members104A and 104B. A bight portion 106 joins the two elongated members at aproximal end of the clamp 100 and biases the two elongated members in anopen position at a distal end of the clamp 100. As used herein, a bightis a loop, bend, hinge, corner angle, hollow, fold, or similarstructure. In some embodiments, the bight portion has one or moreengagement features, such as, for example, a slotted aperture 108 suchas that shown in FIG. 2(b). It should be understood that, in someembodiments, the engagement feature(s) of the bight portion may bereferred to as an attachment feature. A clasp mechanism, in oneembodiment, has a male component 110 disposed on one of the twoelongated members at the distal end, and a female component 112 disposedon the other of the two elongated members at the distal end.

Particularly to partially partition a stomach in performing bariatricsurgery, spacing between the two elongated members 104A and 104B effectstwo or more clamp sections as best shown in FIG. 2(e). At least one ofthe sections is a partition forming section 105A located nearer thedistal end of the clamp 100 than the proximal end of the clamp 100. Atleast another of the sections is a passage forming section 105B locatednearer the proximal end of the clamp 100, such as near the bight portion106, than the distal end of the clamp 100.

In order to reduce injury to the partitioned organ, a padding material116 can be connected to one or more of the two elongated members. Forexample, padding material 116 can connect to the elongated member 104Bat least at a location corresponding to at least part of the partitionforming section. In some embodiments, the padding material can becomposed predominantly of silicone or fully of silicone, or otherpolymer material. It is also envisioned that the opposing limbs of theclamp may be fitted with magnets to facilitate closure.

In some embodiments, the engagement feature at the proximal end of theclamp 100 can be a slotted aperture 108 as shown in FIG. 2(b) having awidth and a length larger in size than the width. The length of theslotted aperture can be oriented perpendicular or angled with referenceto a longitudinal axis of the clamp 100. It is envisioned that othertype engagement features can be employed, such as a socket, a loop, ahook, a clasp, a string, magnet, etc.

In some embodiments, the male component 110 of the clasp at the distalend of the clamp can be an end of the elongated member 104A that flaresaway from a longitudinal axis of the clamp when the clamp is forced to aclosed position. Accordingly, the female component 112 can be a loopattached to the end of the elongated member 104B and disposed to engagethe male component 110 of the elongated member 104A when the clamp isforced to the closed position. This can be seen more clearly inconnection with FIG. 2(e). It is envisioned that other types of claspcomponents can be employed, such as those found in a hinge, such as aliving hinge, hook and loop, spring ring, lobster or trigger, toggle,tube, bolt and bolt hole, screw and threaded aperture, or any other typeof closure arrangement.

Returning to FIG. 1 and referring generally to both FIG. 1 and FIG. 2,the clamp 100, in use, engages with the installation tool by the slottedaperture 108. For example, the installation tool 102 has an elongatedmember, such as a pull-rod 138, having a proximal end and a distal endthat has an engagement feature. The distal end of the elongated memberof the installation tool 102 engages with the proximal end of the clamp100 through the slotted aperture 108 of the bight portion 106. In someembodiments, the engagement feature takes the form of a T-bar 118. ThisT-bar 118 is sized and shaped to allow insertion thereof through theslotted aperture 108 to engage the clamp 100. It is envisioned thatanother engagement features may have an X-shape, and be sized forinsertion through an X-shaped slot in the clamp. Other shapes are alsopossible.

The installation tool 102 may include a lever radially engaged with thepull-rod at its proximal end at a handle 122 that may be configured as athumbwheel 120 that extends out of the handle 122 of the installationtool 102 through an aperture. While the T-bar 118 is inserted throughthe slotted aperture 108, actuating the thumbwheel 120 can cause theT-bar 118 to rotate ninety degrees as illustrated in one embodiment froma first position shown in FIG. 2(c) and in a second position as shown inFIG. 2(d).

At this point, retracting the pull rod, which may be achieved bysqueezing a trigger 128 to retract the pull rod, forces the proximal endof the clamp 100 up against and progressively further between guidemembers of the surgical clamp installation tool 102, such as a pair ofwedges 124A and 124B, formed in the articulating head 126 of theinstallation tool 102 (see FIG. 2(b)). A curvature or incline impartedto the articulating head of the installation tool 102 by the pair ofwedges can be keyed to a curvature or incline of the bight portion 106of the clamp 100 in such a way that fully or more fully retracting thepull-rod forces the normally open clamp 100 to a closed position such asthat shown in FIG. 2(e).

Turning to FIGS. 2(f)-2(k), the various clamp features can be readilyappreciated. These features include bight portion 106, slotted aperture108, male component 110, female component 112, and padding material 116.It should be readily understood that the padding material 116 can beconfigured as a pair of sleeves as shown, but that other configurationsmay also be employed. Moreover, non-linear shapes may be utilized forvarious types of applications in clamping various types of organs, asdesired.

Turning now to FIG. 3 and referring generally to FIG. 1 and FIG. 3,retraction of the pull-rod of the installation tool 102 is accomplishedby actuation or movement of another lever or trigger that is engaged tothe proximal end of the pull-rod, such as through an axial engagement.This lever can be configured as the trigger 128 that extends out of thehandle 122 through an aperture or slotted opening. The shape of thehandle and disposition of the trigger are, preferably, ergonomicallyconfigured to allow the surgeon to hold the installation tool parallelto the ground near waist level to grip the handle 122 and the trigger128 in one hand. The thumbwheel 120 is disposed to be within easy reachof the thumb of that hand to facilitate holding of the clamp 100 by thesurgeon in the other hand while engaging the clamp to the articulatinghead 126. The thumbwheel 120 may be conveniently adjusted to rotate theT-bar 118 to a desired position to lock the T-bar 118 to the clamp 100at the bight portion 106 through the slotted aperture 108. In oneembodiment, the thumbwheel 120 may rotate the T-bar 118 by ninetydegrees.

Once the surgeon has rotated and retracted the pull-rod using T-bar 118and trigger 128 with one hand, the surgeon's other hand becomes free forother tasks, such as actuating yet another lever protruding from thehandle 122 and configured, for example, as a dial 130. With the clamp100 pulled closed or partially closed against the pair of wedges, thehead 126 can be articulated from side to side by rotating this dial 130.The motion of the articulating head 126 through rotation of the dial 130is illustrated in one embodiment in the top view of the installationtool 102 in FIG. 3(b) at arrow 300 showing a range of motion orarticulation in one embodiment.

Turning now to FIG. 4, in some embodiments, turning the dial 130 canturn a hub 132 or connector inside or adjacent the handle 122 that isconnected to a pair of guidelines 134A and 134B. These guidelines 134Aand 134B, together with pull-rod 138, may extend through an elongated,rigid sleeve, such as a cylindrical tube 136, for connection on eitherside of a swivel mount of the articulating head 126. It is envisionedthat the guidelines can be flexible or rigid, that the cylindrical tube136 can be rigid or semi-rigid, and that the pull-rod 138 can be rigidor semi-rigid. By semi-rigid, it is meant that the pull-rod 138 can beflexible or partially flexible at least in the plane of articulationalong at least part of its length near the distal end of theinstallation tool 102, but still axially and rotationally rigid orsemi-rigid along its length. Thus, when the installation tool 102 andclamp 100 are held parallel to the ground, the pull-rod 138 can berotated and retracted by actuation of the thumbwheel 120 and trigger128, and the head 126 can be articulated in a plane orthogonal to thegravity vector by manipulation of the dial 130. The plane ofarticulation may be adjustable in certain embodiments, or may be set ina desired plane that is not orthogonal to the gravity vector.

Turning now to FIG. 5, other embodiments of the clamp 200 andinstallation tool 202 can include a clamp 200 made of multiple pieces, alonger main tube 204, and a thumb lever 206 on the dial 130 toarticulate the head of the tool 102 that is attached to the clamp 200.In some embodiments, the clamp 200 can be a three-piece clamp. A ratchetrelease 208 can also be provided on the installation tool 202 that, whenpressed, allows the pull rod to extend, which in turn will release theclamp 200 allowing it to reopen. In other words, as the surgeon presseson the trigger 210, causing the pull-rod to retract and the clamp 200 toclose, a ratchet mechanism catches the trigger 210 in the pressed-inposition. Thus, the pull-rod will remain retracted and clamp 200 willnot reopen even if the surgeon releases pressure on the trigger 210.

Turning now to FIG. 6, and referring generally to FIGS. 6A-6D, one pieceof a three-piece clamp can be a rigid member 212 having a male clasp end214. As will be described further below with reference to FIG. 9, thisrigid member 212 serves as one of the elongated members of the clamp 200for forming the partition that divides the stomach. It can be made ofplastic, metal, or any other rigid material. An example material ishardened titanium. FIG. 6(c) demonstrates an exemplary contour of maleclasp end 214, while FIG. 6(d) demonstrates an exemplary contour rigidmember 212. It should be readily understood that the exemplary contourof rigid member 212 renders it concave on an inner surface to bedisposed toward an outer surface of an organ to be clamped, and convexon an outer surface for engagement with a spring component. However,other shapes may be used as desired.

Turning next to FIG. 7, and referring generally to FIGS. 7A-7D, anotherpiece of the three-piece clamp can be a rigid member 216 having a femaleclasp end 218 that includes a hinged loop 220. As will be describedfurther below with reference to FIG. 9, this rigid member 216 serves asone of the elongated members of the clamp for forming the partition thatdivides the stomach. It can be made of plastic, metal, or any otherrigid material. An example material is hardened titanium. Similarly, theloop 220 can be made of various materials, an example of which istitanium wire.

Turning next to FIG. 8, and referring generally to FIGS. 8A-8D, a thirdpiece of the three-piece clamp can be a spring member 222 having aslotted bight portion 224. As will be further described below withreference to FIG. 9, the spring member engages with the rigid members toform the clamp and provides the bight portion that permits formation ofa passage between the two partitioned regions of the clamped stomach. Itcan be made of plastic, metal, or any other springy material. An examplematerial is spring tempered titanium.

Turning now to FIG. 9, and referring generally to FIGS. 9A-9D, thethree-piece clamp can be assembled by engaging the rigid members 212 and216 to the spring member 222. For example, the rigid members can bewelded or coupled to arms of spring member at various locations 226. Inone embodiment, the rigid members 212 and 216 can be attached tointerior surfaces of the arms of spring member 222, with the loop 220arranged to hinge towards and engage the male clasp end 214 of thedistal end of rigid member 212. Thus, the rigid members 212 and 216 areemployed to form a partition, while the spring member 222 forms apassage between the partitioned regions of an organ or body as shown inFIG. 10. These rigid members 212 and 216 may be of non-uniform thicknessto accommodate gradual closing of the clamp from the proximal endtowards the distal end in such a manner that a non-uniform thickness ofan organ, such as walls of a stomach, can be clamped without injury.Alternatively or additionally, sleeves of padding material can be slidover the arms of the clamp, and the padding material can be ofnon-uniform thickness as desired. It is envisioned that rigid members212 and 216 and padding material of varying lengths, contours, andthicknesses may be provided to accommodate needs of different patientsas desired.

Turning now to FIG. 10, some embodiments of the surgical clampinstallation tool can be used to install the clamp 100 within anabdominal cavity in order to perform bariatric surgery. In particular,the clamp can be positioned, closed, and latched to partition thestomach into a small vertical portion or pouch 500 and an excludedsection 502. The vertical pouch 500 receives food at 504, but the foodis not able to enter the excluded section 502. Using the installationtool 102 (or 202) to engage with the bight portion 106 of the clamp 100,the clamp 100 may be installed in a substantially vertical position onthe stomach in one embodiment. That is, if the human patient having theclamp 100 installed were to stand upright, the longitudinal axis of theclamp 100 would be substantially parallel to the gravity vector. Thus, apassage forming section formed in the bottom of the stomach by the clampallows gastric juices to flow at 506 from the excluded section 502 intothe vertical pouch 500.

Turning to FIG. 11, a method for clamping an internal organ can includeinserting a surgical clamp through an opening into a body of a livingorganism at block 150. Then the two elongated members of the surgicalclamp are positioned on opposite sides of an internal organ of theliving organism at block 152. At block 154, closing and latching thesurgical clamp to partition a cavity inside the internal organ includesclamping the exterior of the internal organ with the two elongatedmembers.

As mentioned above, the internal organ can be a human stomach. In thiscase, closing and latching the clamp can include installing the clamp ina substantially vertical or angled position with a passage formingsection of the clamp located towards a bottom of the stomach. Thispositioning can create a small, vertical stomach pouch and thereby limitthe intake of food into an excluded section or portion of the stomach,but still allow gastric juices from the excluded portion of the stomachto flow into the vertical stomach pouch. This partitioning can alter theproduction of hormones, enzymes and chemicals that affect metabolism,energy levels, hunger, digestion, and absorption of nutrients that areaffected by exclusion of gastric fundus and body of the stomach by thepartitioning. Sheathing the elongated members of the clamp in siliconepadding material along a majority of their length is intended to reducetrauma and/or necrosis of the stomach or other internal organ and enablesuccessful reversal of the surgery. Thus, the method can further includereversing the surgery by removing the clamp.

Inserting the surgical clamp can include performing natural orificetransluminal endoscopic surgery (NOTES). Alternatively, or additionally,it can include performing a combination of NOTES and an assistant trocarplaced into an abdominal cavity. This combination can include two ormore of a conventional, laparoscopic, NOTES, and one port technique. TheNOTES technique can include at least one of transgastric, transvaginal,transrectal, transcolonic, or combinations thereof. The one porttechnique is used for the introduction of several instruments, andencompasses a one port abdominal (including umbilical), perineal,retroperitoneal approaches, or combinations thereof.

Turning to FIG. 12, a method for clamping an internal organ can includeengaging a surgical clamp to a head of a surgical clamp installationtool at block 160. At block 162, the surgical clamp installation toolcan be employed to close the clamp and insert the clamp through anopening in a body cavity of a living organism. Then the tool can beemployed at block 164 to reopen the clamp and to position elongatedmembers of the clamp on opposite sides of an internal organ within thebody cavity. Next, at block 166, the tool can be employed to close theclamp upon the internal organ and thereby partition a cavity inside theinternal organ. The limbs, arms, or elongated members of the clamp closein such a fashion as causing a gradual diminishing space between the twolimbs, as the space opening extends proximally, accounting for thedifferent thickness of the stomach. The clamp closes in a fashion thatexerts enough pressure to maintain the opposite walls closed to eachother without creating damage/trauma/ischemia to the stomach or otherorgan walls themselves. Then at block 168, the clamp can be latched tofix it in position to partition the internal organ and the cavity insidethe internal organ. Also, at block 170, the clamp can be disengaged fromthe head of the surgical clamp installation tool, and the tool can beretracted from the body cavity at block 172. It is envisioned that theclamp may be configured to latch automatically when the clamp is fullyclosed. Alternatively, the tool may first be disengaged and removed, andthe clamp subsequently latched using an additional tool. Moreover,additional steps may be employed to secure the clamp in place, such asusing sutures.

As already described above, padding material can be employed on surfacesof the elongated members of the surgical clamp to reduce damage to theinternal organ that would prevent reversal of the surgical procedure. Inother embodiments, the thickness or surface contour of the elongatedmembers or arms of the surgical clamp may be provided to align with theparticular organ or body being clamped so as to provide the desiredpressure or force at each location of the organ or body being clamped.Additionally, engaging the surgical clamp to the head of the surgicalclamp installation tool may include passing a T-bar adjacent the end ofa pull rod of the installation tool through a slotted aperture formed ina bight portion of the clamp, and rotating the T-bar using a lever ordial. Also, employing the surgical clamp installation tool to close andreopen the clamp may include operating a lever or trigger on a handle ofthe installation tool to pull and release the pull rod. Further,employing the surgical clamp installation tool to position the elongatedmembers of the surgical clamp may include manipulating a dial on ahandle of the installation tool to articulate the head from side to sidein a desired plane(s).

Turning now to FIG. 13, another embodiment of a surgical clamp 600 andsurgical installation tool 602 is similar in structure and function tothose embodiments described above. One notable difference from theembodiments previously described is that the articulating head 604 ofthe surgical installation tool 602 is keyed with a curvature or radiusconfigured to hold the clamp 600 securely in place while permitting theclamp 600 to remain in an open position. This configuration permits asurgeon holding the installation tool 602 in one hand to hold the clamp600 securely in the articulating head 604 of the tool 602 while pressingthe distal ends of the clamp 600 together with the other end for entryto a trocar. Once the distal ends of the clamp 600 have entered thetrocar, the trocar then holds the ends shut, and permitting the surgeonfree use of the other hand. Upon entry to the abdominal cavity, theclamp naturally springs open for engagement with a bodily organ, such asthe stomach, and the surgeon can articulate the head from side to sidewhile it is held securely in the head 604 while still in the openposition. Once in position, the surgeon can close the clamp usingsutures and/or by applying pressure externally or internally using othersurgical tools. Thus, in this particular embodiment, the installationtool 602 may not be employed to close the clamp on an internal organ ofthe patient, but may be employed to hold, insert, and articulate theclamp into position.

Referring now to FIG. 14, clamp 600 can have a three piece designsimilar to that described above. In other words, it can have a springmember 606 that is comprised predominantly of spring steel, and that isengaged with lower and upper rigid members 608 and 610. These rigidmembers 608 and 610 can be comprised primarily of titanium, and they canhave a concavity that increases their rigidity. In addition, sutureholes 612A-612E can be provided in upper rigid member 610, as well as inan upper portion of spring member 606. A surgeon can employ these sutureholes 612 to secure the clamp 600 in place on a stomach or other bodilyorgan. It is envisioned that additional or alternative suture holes 612can be provided, such as in lower rigid member 608 and lower portion ofspring member 606, and that positions of the suture holes 612 can bedifferent from those shown. However, as will be more fully describedbelow with reference to FIGS. 19-27, the placement of suture holes inthe upper rigid member 608 and upper portion of spring member 606 canpermit suturing of the clamp 600 in place prior to application of asilicone sleeve (see FIGS. 19-27) that slides onto the clamp via theun-sutured lower rigid member 608 and lower portion of spring member606. Yet, once the sleeve is installed, it should be understood thatadditional suture holes 612 provided in lower rigid member 608 and/orlower portion of spring member 606 may prove useful in a subsequentapplication of additional sutures.

Turning now to FIGS. 15(a)-15(f) and referring generally thereto, itshould be appreciated that a double row of suture holes 612A-612H can beprovided in spring member 606 and upper rigid member 610, a distalportion of which can exhibit a male clasp feature 614 positioned toengage a female clasp feature, such as a wire loop 616, of lower rigidmember 608. Suture holes 612D and 612E can be positioned on springmember 606 at a location that lies between a position at which upperrigid member 610 is engaged to spring member 606, and a position atwhich a slot 618 is formed in a bight portion of spring member 606. Inthe case that the distal end of upper rigid member 610 exhibits a maleclasp feature 614, such as a planular curvature away from a plane inwhich the upper rigid member 610 predominantly lies, a complimentaryfemale clasp feature can be exhibited by a distal end of lower rigidmember 608, such as the aforementioned rectangular wire loop 616 engagedby a hinge formation 620 provided in the distal end of lower rigidmember 608. It should be readily understood that the same functionalitycan be achieved if upper rigid member 610 exhibits the female claspfeature, and lower rigid member 608 exhibits male clasp feature 614.Thus, the positions of the clasp features can be reversed in otherembodiments.

Turning now to FIG. 16, another additional feature of clamp 600 can be adetent 622 that is formed in hinge formation 620, and that engages wireloop 616 of the female clasp feature. This detent 622 can be positionedon the hinge formation 620 at a location that is most distal when theclamp 600 is held in a closed position, and it can be sized and shapedto hold the wire loop 616 in a lowered position at which the loop 616lies in a plane parallel to a plane in which lower rigid member 608predominantly lies. A similar or identical detent (not shown) can beprovided on an opposite side of hinge formation 620, and it can besimilarly distally positioned to assist in holding the wire loop 616 inthe aforementioned lowered position. This lowered position allows theclamp 600 to be inserted through a trocar and guided to enclose a bodilyorgan, such as a stomach, at which point the aforementioned siliconesleeve (see FIGS. 19-27) can be partially applied. Then, before thesilicone sleeve is fully engaged to the clamp 600, wire loop 616 can beforced out of detent 622 into a raised position at which it engages themale clasp feature 614 of the clamp 600.

Before raising the wire loop 616, it is envisioned that the clamp 600can be pressed into a closed position by use of two or more graspersinserted into the abdominal cavity through additional trocars (i.e.,multiport technique). Then, a suture tag pre-applied to wire loop 616can be used to force wire loop 616 out of detent 622 into the raisedposition, resulting in the wire loop 616 engaging the male clasp feature614 and holding the clamp 600 in the closed position without assistancefrom the two or more graspers. Alternatively or additionally, it isenvisioned that closing and latching of the clamp 600 can be achieved byutilizing any suitable endoscopic surgical tools and techniques as willbe readily apparent to one skilled in the art from the presentdisclosure.

Turning now to FIGS. 17(a)-17(f) and referring generally thereto, anendoscopic surgical installation tool for engaging and manipulating theclamp can be similar to those described above. For example, theinstallation tool can have a handle 650, trigger 652, pull rod, T-bar654, cylindrical tube 656, dial 658 (e.g., with thumb lever), hub,guidelines, and articulating head 604 that are identical or similar tothose described above. However, as previously described, a curvature orincline imparted to the head 604 by wedges of the head 604 can be keyedto a bight portion of the previously described clamp so as to hold theclamp in a fully open or predominantly open position when T-bar 654 hasbeen fully retracted by actuation of trigger 652. Additionally, a latchrelease 660 can be provided that can extend from both sides of handle650 for ergonomic, ambidextrous operation.

Turning now to FIG. 18, the latch release 660 can have a hinged platewith a retention spring that forces the latch release 660 upwards toengage a latch 662 provided at a proximal end of pull rod 664. In use, asurgeon can engage the T-bar to the clamp 600 by rotating the clamp 600and/or installation tool in a common longitudinal axis until the T-barfits through the notch in the bight portion of the clamp 600, and thenrotating the clamp 600 and/or installation tool an integer multiple ofninety degrees until a length direction of the T-Bar is perpendicular toa length direction of the notch. Then, actuation of trigger 652 canretract pull rod until opposing latch surfaces (e.g., edges, extensions,faces, flanges, gouges, hooks, inclines, ledges, lips, notches,overhangs, projections, protrusions, ribs, ridges, skirts, serrations,slits, slots, teeth, wedges, and combinations thereof) of the latch 662and release 660 can catch and hold the pull rod 664 in a fully retractedor predominantly retracted position.

Once the latch 662 is engaged, the clamp 600 is ready to be insertedinto an inflated abdominal cavity through a trocar as described above,and a seal provided between cylindrical tube 656 and clevis 668 canprevent out gassing from the abdominal cavity through the head 604and/or cylindrical tube 656. Alternatively, the seal can be providedanywhere inside cylindrical tube 656. In some embodiments, the seal isachieved by using a circular silicone die having a slit and a hole inthe middle, with the pull rod 664 threaded through the hole.

Once the clamp 600 is in position within the abdominal cavity to encloseand partition the stomach or other organ, pressing down on latch release660 can permit automatic extension of pull rod 664 by action of atorsion spring provided to trigger screw 666 to force de-actuation oftrigger 652. The T-bar can then be disengaged from the clamp by rotatingthe installation tool along its longitudinal axis an integer multiple ofninety degrees and removing it from the trocar. Thus, it should beapparent that, in some embodiments, the pull rod may not be configuredto rotate as in alternative embodiments described above, but only toretract and to extend.

Turning now to FIG. 19, a silicone sleeve 700 can be configured toengage clamp 600. In some embodiments, silicone sleeve 700 can be formedto cover primarily an upper arm and both ends of clamp 600. Thissilicone sleeve 700 can be used as padding to protect surrounding organsfrom irritation or damage. Thickness of the silicone can be varied fordifferent applications, such as partitioning an organ, stomach, orvessel.

Turning now to FIGS. 20-27 and referring generally thereto, the siliconesleeve 700 can have tubular section 702 at a proximal end that slidesonto the lower arm of clamp and can be manipulated into position toencapsulate the previously described bight portion of the clamp. Theclamp can then be closed and latched as described above. Presuming thatthe upper arm of the clamp has already been sutured to the organ,stomach, or vessel, a distal end of the sleeve 700 can then be engagedto encapsulate the distal end of the clamp. For this purpose, the distalend of the sleeve 700 can be configured as a latch cap 704 that is formfitted to the closed latch features (see FIG. 25). A padding strip 706situated between the tubular section 702 and latch cap 704 can be sizedto a length of the clamp so as to be stretched taught across the upperarm of the clamp once the sleeve 700 is installed. A slot engagingfeature 708 formed inside of tubular section 702 can be provided toengage with the previously described slot in the bight portion of theclamp by plugging the slot, and thus hold the tubular section of thesleeve 700 in place on the bight portion of the clamp.

Turning now to FIG. 28, a method of performing surgery can begin at step750 by engaging the previously described clamp to the previouslydescribed surgical installation tool in one or more of the previouslydescribed manners. Thereafter, the clamp can be inserted through atrocar at step 752, and positioned to enclose an organ (e.g., stomach,vessel, etc.) at step 754. Next, at step 756, an upper arm of the clampcan be sutured to the organ though suture holes supplied in the clamp aspreviously described, and the installation tool can be disengaged andremoved from the trocar at step 758. Thereafter, the previouslydescribed silicone sleeve can be slid over a lower arm of the clamp atstep 760 as previously described, and the clamp can be closed andlatched at step 762. Finally, at step 764, a latch cap of the siliconesleeve can be fit over the latch of the clamp, and additional suturescan be applied if desired. It should be understood that the sequence ofthe aforementioned steps can vary in additional or alternativeembodiments, and that additional or alternative steps can be employed aswill be readily apparent to one skilled in the art.

FIGS. 29-40 and the accompanying description disclose variousembodiments of a surgical clamp overmolded in a polymer material. Thesurgical clamp is, in one implementation, a laparoscopically implanteddevice which, when closed and latched or secured, partitions a patient'sstomach into two sections, such as two vertical sections or otherdivisions. The clamp may be installed using standard surgical tools(e.g., clamps, scissors, etc.) and/or, in some embodiments, aninstallation tool, such as one of the installation tools discussedherein. When the clamp is installed, in one installation, the lessercurvature segment of the stomach forms the Magenstrasse, and the greatercurvature segment, including the fundus, is generally excluded fromnutritional contact. In one implementation, the clamp includes, at aproximal end, an aperture with an enlarged radius (generally referred tohereafter as the bight portion or passage-forming section), by whichgastric juices created by the fundus and the body can empty into theatrum. By excluding the fundus, the clamp may alter or reduce hormonessuch as, for example, ghrelin, leading to the patient's loss of hunger.Additionally, the clamp acts as a restrictive procedure by reducing thesize of the Magenstrasse by creating a small lumen for a verticalpassageway of the nutrients along the lesser curvature.

FIG. 29 illustrates an embodiment, wherein the fully or partiallyovermolded surgical clamp is of a one-piece design. The one-piece clamp2900 includes first and second substrate members (shown in FIGS. 30(a),30(b), 31(a) and 31(b)) overmolded in a polymer or elastomer material toform a first elongated portion 2902, a second elongated portion 2904, abight portion 2906, a fastener portion 2908, and an engagement portion2914. As mentioned above, the first and second elongated portions 2902and 2904 serve as a partition-forming section of the clamp 2900.Referring briefly to both FIGS. 29 and 10, when the clamp 2900 isinstalled within an abdominal cavity, the first and second elongatedportions 2902 and 2904 are engaged to partition the stomach into asmall, vertical pouch 500 and an excluded section 502. The bight portion2906 comprises a passage-forming section located towards the proximalend of the clamp 2900. The passage-forming section allows gastric juicesto flow 506 from the excluded section 502 into the vertical pouch 500.

In accordance with the present disclosure, the term overmolded isintended to describe a product wherein underlying substrate material(s)are substantially fully or partially encapsulated, covered, or coatedwith one or more layers of one or more overlying materials. For example,in accordance with the embodiment illustrated in FIG. 29, the first andsecond substrate members comprise the underlying substrate materials,and the overlying polymer or elastomer material comprises the overmoldedmaterial, or overmolding. In some embodiments, the overmolding may be ofa non-uniform thickness or durometer, or positioned in certain areas, toproduce various portions or features (such as a fastener portion,flexible hinge, etc.) and/or to accommodate gradual closing of the clampfrom the proximal end towards the distal end in such a manner that anon-uniform thickness of an organ, such as walls of a stomach, can beappropriately clamped without injury. In some embodiments, theovermolded polymer material may comprise silicone such as, for example,an unrestricted implant-grade silicone. In some embodiments, thesubstrate material may comprise the same material as the overmolding.Additionally, in some embodiments, the substrate material(s) andovermolding material(s) may comprise different or varying materialsand/or durometers.

As shown in FIG. 29, the first and second elongated portions 2902 and2904 are joined by the bight portion 2906 at the proximal end of theclamp 2900. The bight portion 2906 includes a flexible hinge 2918formed, in one implementation, from the polymer overmold, wherein theflexible hinge 2918 permits expansion and movement of the bight portion2906 to accommodate any irregularities in the stomach wall orfluctuations of the passage-forming section when the clamp 2900 isinstalled. The flexible hinge 2918 also allows the clamp 2900 toaccommodate variations in stomach thicknesses without compromising thepressure applied by the clamp 2900, particularly in thepartition-forming section. In some embodiments, the flexible hinge 2918includes one or more attachment features such as, for example, a slottedaperture 2920. The attachment feature may allow the clamp 2900 to beengaged with an installation tool (for example, such as the installationtool shown in FIG. 33) in accordance with the foregoing disclosure. Instill other embodiments, the flexible hinge 2918 may be provided at adesired durometer or elasticity that may be the same as or differentfrom that of the polymer or silicone overmolded portions provided inother areas of the clamp 2900, such as the first and second elongatedportions 2902 and 2904.

When installing the surgical clamp 2900, the clamp 2900 is placed intoposition as explained in greater detail below, and the fastener portion2908 and engagement portion 2914 are used to retain the clamp 2900 in asubstantially closed position. In the embodiment illustrated in FIG. 29,the fastener portion 2908 comprises a strap formed from the overmoldedpolymer or other material and located towards the distal end of thesecond elongated portion 2904. The strap may include one or more primaryopenings 2910 for receiving the engagement portion 2914, and a secondaryopening 2912 used for adjusting or manipulating the fastener portion2908 and/or the second elongated portion 2904. For example, a surgeonmay use a tool (not shown) to engage the secondary opening 2912 toposition the strap such that the engagement portion 2914 engages one ofthe primary openings 2910. In the embodiment illustrated in FIG. 29, theengagement portion 2914 comprises a protrusion, such as a hook or tab,for engaging openings of the fastener portion 2908.

In some embodiments, the clamp 2900 may be adjusted by disengaging theengagement portion 2914 from one of the primary openings 2910, andengaging the engagement portion 2914 with another one of the primaryopenings 2910 to either increase or decrease the spacing between thefirst and second elongated portions 2902 and 2904. In some embodiments,the fastener portion 2908 may be sutured to the first elongated portion2902 using suture pass-through holes 2916, such as those located alongan outside surface of the first elongated portion 2902. Additionally, insome embodiments, once positioned on the stomach, the suturepass-through holes 2916 may be used to suture the clamp 2900 to thestomach walls to avoid displacement. It should be understood that, insome embodiments, sutures may be placed through the overmolding, asdescribed in greater detail below.

Referring now to FIGS. 30(a) and 30(b), the surgical clamp 2900 of FIG.29 is shown from respective side and perspective views, wherein thepolymer material is illustrated semitransparent to show the underlyingfirst substrate member 3001 and second substrate member 3002. As shownin FIGS. 30(a) and 30(b), the first and second substrate members 3001and 3002 may, in some embodiments, comprise the respective first andsecond elongated portions 2902 and 2904, as well as at least a part ofthe bight portion 2906. Additionally, in some embodiments, the firstsubstrate member 3001 may also comprise at least a portion of theengagement feature 2914.

FIGS. 31(a) and 31(b) illustrate the respective first and secondsubstrate members 3001 and 3002 comprising the one-piece clamp 2900illustrated in FIGS. 29, 30(a) and 30(b). In some embodiments, the firstand second substrate members 3001 and 3002 each comprise a 3 mm-thicktitanium substrate. As shown in FIG. 31(a), the first substrate member3001 may include a tab or a hook 3102 comprising at least a portion ofthe engagement feature 2914, a first section 3104 comprising a part ofthe first elongated portion 2902, and a second section 3106 comprising apart of the bight portion 2906. As shown in FIG. 31(b), the secondsubstrate member 3002 may include a first section 3108 comprising a partof the second elongated portion 2904 and a second section 3110comprising a part of the bight portion 2906. It should be understoodthat the dimensions and materials comprising the substrate membersprovided herein are merely examples. It is envisioned that the substratemembers may be of various thicknesses and lengths, and may be comprisedof various biocompatible materials such as titanium or biocompatiblepolymer resins such as polyether ketone ketone (PEKK) or polyether etherketone (PEEK).

In accordance with the embodiment illustrated in FIGS. 29, 30(a), 30(b),31(a) and 31(b), the polymer overmolded portion of the clamp 2900 is a1.5 mm-thick layer of polymer material (e.g., silicone) encapsulatingthe first and second substrate members 3001 and 3002. The flexible hinge2918 and fastener portion 2908 are formed from the polymer material, andare approximately 6 mm thick to provide a substantially consistentthickness along the surgical clamp 2900. However, as previouslydiscussed, in some embodiments, the polymer material comprising orovermolding one or more portions of the clamp 2900 may have anon-uniform thickness or application. It should be appreciated that theforegoing dimensions are merely examples and are not intended to limitor define any aspects of the clamp or portions thereof.

FIG. 32 illustrates another embodiment of a one-piece surgical clamp3200 comprised of first and second substrate members overmolded in apolymer material. The clamp 3200 includes a first elongated portion3202, second elongated portion 3204, bight portion 3206 with flexiblehinge 3208 and attachment feature 3210, a fastener portion 3212 and anengagement feature 3214. The clamp 3200 illustrated in FIG. 32 issimilar to the clamp 2900 illustrated in FIG. 29, except, for example,that the fastener portion 3212 of the clamp 3200 omits the secondaryopening 2912.

Referring now to FIG. 33, another example embodiment of an installationtool 3300 is illustrated. The installation tool 3300 is similar to thosediscussed above, and may be used in a similar manner to engage andinstall certain embodiments of the surgical clamps illustrated in FIGS.29-32. Using the installation tool 3300, the clamp may be engaged (viathe attachment feature of the bight portion), placed in the abdominalcavity (e.g., via a trocar) and positioned with the first and secondelongated portions on opposite sides of the stomach, where the clamp islatched, closed, fastened, secured, or otherwise installed to at leastpartially partition a cavity inside the stomach as described above.

FIGS. 34(a), 34(b) and 34(c) illustrate various views of yet anotherembodiment of a one-piece surgical clamp 3400 comprised of first andsecond substrate members 3401 and 3402 overmolded in a polymer material3403. The clamp 3400 includes a first elongated portion 3404, secondelongated portion 3406, bight portion 3408 with flexible hinge 3410, afastener portion 3412 and engagement features 3414 and 3416. The clamp3400 illustrated in FIGS. 34(a), 34(b) and 34(c) is similar to the clamp3200 illustrated in FIG. 32. The fastener portion 3412 of the clamp 3400includes, for example, rounded primary openings 3418, and the bightportion 3412 omits an attachment feature. Additionally, the clamp 3400incorporates first and second engagement features 3414 and 3416, whereinthe first and second engagement features 3414 and 3416 include a raisedmember and a retaining loop, respectively, formed from the polymerovermolding 3403. In some embodiments, the raised member may also beformed, at least partially, from the first substrate member.

In accordance with the embodiment illustrated in FIGS. 34(a), 34(b) and34(c), the clamp 3400 may be inserted to an abdominal cavity through atrocar, positioned with the first and second elongated portions 3404 and3406 on opposite sides of the stomach, and closed and secured byengaging one of the primary openings 3418 with the raised member of thefirst engagement feature 3414, and securing the fastener portion 3412under the retaining loop of the second engagement feature 3416. Inaccordance with the present embodiment, the inserting, positioning,closing and securing steps may be performed using surgical tools (e.g.,clamps, forceps, scissors, etc.). However, it should be appreciated thatthe bight portion 3408 of the clamp 3400 may be modified to include anattachment feature, such as that provided in clamp 2900 or 3200, toallow for the clamp 3400 to be engaged and installed using a surgicalclamp installation tool, such as that provided in FIG. 33.

FIG. 35 illustrates another embodiment of a one-piece surgical clamp3500 comprised of first and second substrate members overmolded in apolymer material. The clamp 3500 includes a first elongated portion3502, second elongated portion 3504, bight portion 3506 with flexiblehinge 3508, a fastener portion 3510 and engagement features 3512, 3514and 3516. The clamp 3500 is similar to the clamp 3400 illustrated inFIGS. 34(a), 34(b) and 34(c). The clamp 3500 incorporates an additionalengagement member 3516 comprising a retaining loop formed from thepolymer overmolding for receiving the fastener portion 3510. The clamp3500 is installed in a manner similar to the clamp 3400 and may bemodified to include an attachment feature, such as that provided inclamp 2900 or 3200, to allow for the clamp 3500 to be engaged andinstalled using a surgical clamp installation tool, such as thatprovided in FIG. 33. It should be appreciated that the variousembodiments discussed herein may be modified to include differentnumbers and combinations of engagement features and fastener portionopenings without departing from the scope of the present disclosure asset forth in the aspects below.

Referring now to FIG. 36, a method for clamping an internal organ caninclude inserting a surgical clamp through an opening (e.g., using atrocar) into a body of a living organism at block 3610. Then the firstand second elongated portions of the surgical clamp are positioned onopposite sides of an internal organ of the living organism at block3620. At block 3630, closing and securing the surgical clamp topartition a cavity inside the internal organ includes clamping theexterior of the internal organ with the two elongated portions.

As mentioned above, the internal organ can be a human stomach. In thiscase, closing and securing the clamp can include installing the clamp ina substantially vertical or angled position with a passage-formingsection of the clamp located towards a bottom of the stomach. Thispositioning can create a small, vertical stomach pouch and thereby limitthe intake of food into an excluded section or portion of the stomach,but still allow certain gastric juices from the excluded portion of thestomach to flow into the vertical stomach pouch. This partitioning canalter the production of hormones, enzymes and chemicals that affectmetabolism, energy levels, hunger, digestion, and absorption ofnutrients that are affected by exclusion of gastric fundus and body ofthe stomach by the partitioning. The polymer overmolding of the clampreduces trauma and/or necrosis of the stomach or other internal organ,thereby enabling successful reversal of the surgery. Thus, the abovemethod can further include reversing the surgery by removing the clamp.

Inserting the surgical clamp can include performing natural orificetransluminal endoscopic surgery (NOTES). Alternatively, or additionally,it can include performing a combination of NOTES and an assistant trocarplaced into an abdominal cavity. This combination can include two ormore of a conventional, laparoscopic, NOTES, and one port technique. TheNOTES technique can include at least one of transgastric, transvaginal,transrectal, transcolonic, or combinations thereof. The one porttechnique is used for the introduction of several instruments, andencompasses a one port abdominal (including umbilical), perineal,retroperitoneal approaches, or combinations thereof.

Referring now to FIG. 37, a method for clamping an internal organ caninclude engaging a surgical clamp, such as a bariatric clamp, to a headof a surgical clamp installation tool at block 3710. At block 3720, thesurgical clamp installation tool can be employed to close the clamp andinsert the clamp through an opening in a body cavity of a livingorganism. Then the tool can be employed at block 3730 to reopen theclamp and to position the first and second elongated portions of theclamp on opposite sides of an internal organ within the body cavity.

Next, at block 3740, the tool can be employed to close the clamp uponthe internal organ and thereby partition a cavity inside the internalorgan. The limbs, arms, or elongated portions of the clamp close in sucha fashion as causing a gradual diminishing space between the twoelongated portions, as the space opening extends proximally, accountingfor the different thickness of the stomach. The clamp closes in afashion that exerts enough pressure to maintain the opposite wallsclosed to each other without creating any undue damage/trauma/ischemiato the stomach or other organ walls themselves. Then at block 3750, theclamp can be latched or otherwise secured to fix it in position topartition the internal organ and the cavity inside the internal organ.Also, at block 3760, the clamp can be disengaged from the head of thesurgical clamp installation tool, and the tool can be retracted from thebody cavity at block 3770. In some embodiments, the clamp may be latchedor secured prior to or after disengaging and removing the surgical clampinstallation tool. In such embodiments, the securing of the clamp may beperformed using surgical tools alone or in combination with theinstallation tool. Alternatively, the tool may first be disengaged andremoved, and the clamp subsequently latched using the additionalsurgical tools. Moreover, additional steps may be employed, eitherbefore or after the clamp is secured, to secure and position the clampin place, such as using sutures.

As described above, the polymer overmolding of the surgical clampreduces damage to the internal organ that would prevent or significantlydecrease the likelihood of reversal of the surgical procedure. In someembodiments, the thickness or surface contour of the elongated portionsof the surgical clamp may be provided to align with the particular organor body being clamped so as to provide the desired pressure or force ateach location of the organ or body being clamped. Additionally, engagingthe surgical clamp to the head of the surgical clamp installation toolmay include passing a T-bar adjacent the end of a pull rod of theinstallation tool through a slotted aperture formed in a bight portionof the clamp, and rotating the T-bar using a lever or dial. Also,employing the surgical clamp installation tool to close and reopen theclamp may include operating a lever or trigger on a handle of theinstallation tool to pull and release the pull rod. Further, employingthe surgical clamp installation tool to position the elongated portionsof the surgical clamp may include manipulating a dial on a handle of theinstallation tool to articulate the head from side to side in a desiredplane(s).

FIGS. 38, 39(a), 39(b) and 39(c) illustrate an embodiment of the presentdisclosure, wherein the polymer overmolded surgical clamp is of atwo-piece design. FIG. 38 illustrates a perspective view of thetwo-piece clamp 3800, and FIGS. 39(a), 39(b) and 39(c) illustratevarious views of the clamp 3800, wherein the polymer overmold isillustrated semitransparent to show the underlying first substratemember 3901 and second substrate member 3902. FIG. 39(a) illustrates aprofile view of the clamp 3800; FIG. 39(b) illustrates a top-down viewof the clamp 3800; and FIG. 39(c) illustrates a cross-sectional view ofthe clamp 3800 taken along line A-A of FIG. 39(b).

The two-piece clamp 3800 includes first and second substrate members3901 and 3902 (shown in FIGS. 39(a), 39(b) and 39(c)) overmolded in apolymer material to form a first elongated member 3802 and a separate,second elongated member 3804. The first elongated member 3802 includes afirst bight portion 3806 located towards a proximal end of the clamp3800, and a first elongated portion 3808 located towards a distal end ofthe clamp 3800. The second elongated member 3804 includes a second bightportion 3810 located towards the proximal end of the clamp 3800 and asecond elongated portion 3812 located towards the distal end of theclamp 3800. When the clamp is installed, the first and second bightportions 3806 and 3810 comprise a passage-forming section at theproximal end of the clamp 3800, and the first and second elongatedportions 3808 and 3812 comprise a partition-forming section at thedistal end of the clamp 3800. Referring briefly to both FIGS. 38 and 10,when the clamp 3800 is installed within an abdominal cavity, the firstand second elongated portions 3808 and 3812 are engaged to partition thestomach into a small, vertical pouch 500 and excluded section 502, andthe first and second bight portions 3806 and 3810 are engaged to form apassage that allows gastric juices to flow 506 from the excluded section502 into the vertical pouch 500.

As shown in FIGS. 38, 39(a), 39(b) and 39(c), the first elongated member3802 includes first and second fastening portions 3814 and 3816 formedat least partially from the polymer overmold at opposite ends of thefirst elongated member 3802. The second elongated member 3804 includesfirst and second receiving portions 3818 and 3820 formed from thepolymer overmold at opposite ends of the second elongated member 3804,and retention features 3822, 3824, 3826 and 3828 formed at an outersurface of the second elongated member 3804. It should be understoodthat, in some embodiments, the first and second receiving portions 3818and 3820 may be formed from the polymer overmold, or a combination ofthe second substrate material and polymer overmold. Similarly, in someembodiments, the retention features 3822, 3824, 3826 and 3828 may beformed from the polymer overmold, or a combination of the secondsubstrate material and polymer overmold, as shown in FIG. 39(c).

When installing the clamp 3800, the first and second elongated members3802 and 3804 are inserted into the abdominal cavity (for example, usinga trocar) and positioned on opposite sides of the stomach. Then, thefirst and second fastening portions 3814 and 3816 are each fed throughrespective first and second receiving portions 3818 and 3820. A spacingbetween the bight portions 3806 and 3810 defines the passage formed atthe bottom of the stomach and affects the pressure applied to theinternal organ, whereas a spacing between the elongated portions 3808and 3812 affects the pressure applied to the stomach by thepartition-forming section of the clamp 3800. The spacing between thefirst and second bight portions 3806 and 3810 may be independentlycontrolled primarily by adjusting the length of the first fasteningportion 3814 fed through the first receiving portion 3818. Similarly,the spacing between the first and second elongated portions 3808 and3812 may be independently controlled primarily by adjusting the lengthof the second fastening portion 3816 fed through the second receivingportion 3820. Once the desired spacing is achieved, the clamp 3800 isclosed, latched or otherwise secured by engaging the first and secondfastening portions 3814 and 3816 with the outer surface of the secondelongated member 3804 using the retention features 3822, 3824, 3826 and3828. The clamp 3800 may be adjusted or uninstalled by reversing theinstallation procedure. Additionally, in some embodiments, installation,removal, and/or adjustment of the clamp 3800 may be performed usingstandard surgical tools (e.g., forceps, clamps, scissors, etc.).

In the embodiment illustrated in FIGS. 38, 39(a), 39(b) and 39(c),retention features 3822 and 3828 comprise retention loops, and retentionfeatures 3824 and 3826 comprise raised members. The first fasteningportion 3814 is fed through the first receiving portion 3818 and underthe retaining loop 3822. The first fastening portion 3814 includes oneor more openings 3830 operable to receive the raised member 3824. Oncethe first fastening portion 3814 is fed through the retaining loop 3822,it is secured via a friction fit using the raised member 3824 and one ofthe openings 3830. Similarly, the second fastening portion 3816 is fedthrough the second receiving portion 3820 and under the retaining loop3828. The second fastening portion 3816 includes one or more openings3832 operable to receive the raised member 3826. Once the secondfastening portion 3816 is fed through the retaining loop 3828, it issecured via a friction fit using the raised member 3826 and one of theopenings 3832. In some embodiments, the first and second fasteningportions 3814 and 3816 may be further secured by suturing the fasteningportions 3814 and 3816 to the second elongated member 3804 usingsuturing holes (not shown) formed within the second substrate member andpolymer overmolding.

As briefly discussed above, the spacings at the passage-forming andpartition-forming sections of the clamp may be adjusted independent ofeach other. Thus, the two-piece surgical clamp 3800 permits customizedinstallation and adjustment of the surgical clamp 3800 by permitting oneend of the clamp (i.e., the passage-forming section or thepartition-forming section) to be adjusted without having to adjust theother end. This allows a surgeon or other medical personnel to controlthe clamping pressure at each end of the device regardless ofdifferences in thickness of the stomach from one end of the clamp 3800to the other.

FIG. 40 illustrates another example embodiment of a two-piece surgicalclamp 4000. The two-piece clamp 4000 includes first and second substratemembers overmolded in a polymer material to form a first elongatedmember 4002 and a separate, second elongated member 4004. The firstelongated member 4002 includes a first bight portion 4006 locatedtowards a proximal end of the clamp 4000, and a first elongated portion4008 located towards a distal end of the clamp 4000. The secondelongated member 4004 includes a second bight portion 4010 locatedtowards the proximal end of the clamp 4000 and a second elongatedportion 4012 located towards the distal end of the clamp 4000. When theclamp is installed, the first and second bight portions 4006 and 4010comprise a passage-forming section at the proximal end of the clamp4000, and the first and second elongated portions 4008 and 4012 comprisea partition-forming section at the distal end of the clamp 4000. Thespacing between the bight portions 4006 and 4010 defines the passageformed at the bottom of the stomach and affects the pressure applied tothe internal organ, whereas the spacing between the elongated portions4008 and 4012 affects the pressure applied to the stomach by thepartition-forming section of the clamp 4000.

The first elongated member 4002 includes first and second fasteningportions 4014 and 4016 formed from the polymer overmold at opposite endsof the first elongated member 4002. The second elongated member 4004includes first and second receiving portions 4018 and 4020 formed fromthe polymer overmold at opposite ends of the second elongated member4004. The embodiment illustrated in FIG. 40 is similar to that shown inFIGS. 38, 39(a), 39(b) and 39(c), except that the retention feature ofthe embodiment illustrated in FIG. 40 is embodied as a ratchet-typefeature, wherein each of the first and second fastening portions 4014and 4016 each include a plurality of “teeth” 4022 designed to engage therespective receiving portions 4018 and 4020 of the second elongatedmember 4004.

When installing the clamp 4000, the first and second elongated members4002 and 4004 are inserted into the abdominal cavity (for example, usinga trocar) and positioned on opposite sides of the stomach. The first andsecond fastening portions 4014 and 4016 are then fed through respectivefirst and second receiving portions 4018 and 4020. The teeth 4022 oneach of the fastening portions 4014 and 4016 are designed to flex topermit the feeding of respective fastening portion 4014 or 4016 throughthe respective receiving portion 4018 or 4020, and to engage therespective receiving portion 4018 or 4020 to retain the second elongatedmember 4004, thereby securing the clamp 4000 in a closed position. Insome embodiments, the first and second elongated members 4002 and 4004may be further secured by suturing the first and second elongatedmembers 4002 and 4004 to the stomach using suturing holes (not shown)formed within the elongated members.

The spacing between the first and second bight portions 4006 and 4010may be independently controlled primarily by adjusting the length of thefirst fastening portion 4014 fed through the first receiving portion4018. Similarly, the spacing between the first and second elongatedportions 4008 and 4012 may be independently controlled primarily byadjusting the length of the second fastening portion 4016 fed throughthe second receiving portion 4020. The clamp 4000 may be readjusted oruninstalled by disengaging the teeth 4022 of the fastening portions 4014and 4016 from the respective receiving portions 4018 and 4020, andadjusting or removing the fastening portions 4014 and 4016 from thereceiving portions 4018 and 4020. In some embodiments, once the clamp4000 is installed, excess length of the first and second fasteningportions 4014 and 4016 may be removed, for example, using scissors orother cutting instruments. In some embodiments, installation, removal,and/or adjustment of the clamp 4000 may be performed using standardsurgical tools (e.g., forceps, clamps, scissors, etc.).

Like the clamp 3800 of FIG. 38, the two-piece clamp 4000 of FIG. 40allows for independent adjustment of the spacings at the passage-formingand partition-forming sections of the clamp 4000. Thus, the two-piecesurgical clamp 4000 permits customized installation and adjustment ofthe surgical clamp 4000 by permitting one end of the clamp (i.e., thepassage-forming section or the partition-forming section) to be adjustedwithout having to adjust the other end. This allows a surgeon or othermedical personnel to control the clamping pressure at each end of thedevice regardless of differences in thickness of the stomach from oneend of the clamp 4000 to the other.

Embodiments of the polymer overmolded two-piece surgical clamp may beinstalled as described above with respect to the flow-chart illustratedin FIG. 36. Additionally, the polymer overmolding of the two-piecesurgical clamp reduces or prevents damage to the internal organ thatwould prevent or complicate reversal of the surgical procedure. In someembodiments, the thickness or surface contour of the elongated portionsof the surgical clamp may be provided to align with the particular organor body being clamped so as to provide a desired pressure or force ateach location of the organ or body being clamped. It should beappreciated that, in some embodiments, the first and second elongatedmembers may be formed entirely from the polymer or elastomer material orresign and do not include an underlying substrate member.

It should be understood that one or more of the various fasteningportions and retention features of the two-piece overmolded surgicalclamp, such as the ratchet-like feature of the clamp 4000, the raisedmembers and retention loops of the clamp 3800, or various combinationsthereof may, in some embodiments, be incorporated in the one-pieceovermolded surgical clamp. Additionally, in some embodiments, one ormore of the engagement features of the one-piece overmolded surgicalclamp may be incorporated in the two-piece overmolded surgical clamp.Furthermore, it should be appreciated that, in some embodiments, theone-piece surgical clamp may be a single, integrated unit or, in otherembodiments, may be a modular unit formed of multiple pieces or partscombined to form the one-piece surgical (bariatric) clamp. It shouldalso be appreciated that, in some embodiments, each of the piecescomprising the two-piece surgical clamp may include a single, integratedpiece or, in other embodiments, may be a modular piece formed ofmultiple parts combined to form a piece of the two-piece surgical(bariatric) clamp.

FIGS. 41-81 and the accompanying description disclose variousembodiments of a bariatric clamp (or surgical clamp) overmolded in apolymer material or are otherwise provided in support of suchdisclosure. The bariatric clamp is, in one implementation, alaparoscopically implanted device which, when closed and latched orsecured, partitions a patient's stomach into two sections, such as twovertical sections or other divisions. The clamp may be installed usingstandard surgical tools (e.g., clamps, scissors, etc.) as furtherdescribed below. When the clamp is installed, in one installation, thelesser curvature segment of the stomach forms the Magenstrasse, and thegreater curvature segment, including the fundus, is generally excludedfrom nutritional contact. In one implementation, the clamp includes, ata proximal end, an aperture with an enlarged radius (generally referredto as the bight portion or passage-forming section), by which gastricjuices created by the fundus and the body can empty into the atrum. Byexcluding the fundus, the clamp may alter or reduce hormones such as,for example, ghrelin, leading to the patient's loss of hunger.Additionally, the clamp acts as a restrictive procedure by reducing thesize of the Magenstrasse by creating a small lumen for a verticalpassageway of the nutrients along the lesser curvature.

FIGS. 41(a)-41(e) illustrate various views of an embodiment of anovermolded bariatric clamp 4100. The clamp 4100 includes first andsecond substrate members 4101 and 4103 (shown dashed in FIGS. 41(a) and41(e) and similar to those shown in FIGS. 30(a), 30(b), 31(a) and 31(b))overmolded in a polymer or elastomer material to form a first elongatedportion 4102, a second elongated portion 4104, a bight portion 4106, afastener portion 4108, and an engagement portion 4114. As discussedabove, the first and second elongated portions 4102 and 4104 serve as apartition-forming section of the bariatric clamp 4100. Referring brieflyto both FIGS. 41(a) and 10, when the clamp 4100 is installed within anabdominal cavity, the first and second elongated portions 4102 and 4104are engaged to partition the stomach into a small, vertical pouch 500and an excluded section 502. The bight portion 4106 comprises apassage-forming section located towards the proximal end of the clamp4100. The passage-forming section allows gastric juices to flow 506 fromthe excluded section 502 into the vertical pouch 500.

As shown in FIGS. 41(a)-41(e), the first and second elongated portions4102 and 4104 are joined by the bight portion 4106, which is disposedgenerally at the proximal end of the clamp 4100. The bight portion 4106includes a flexible hinge 4118 formed, in one implementation, from thepolymer overmold. The flexible hinge 4118 allows the clamp 4100 to bepositioned in a variety of positions ranging from a substantially closedposition illustrated in FIGS. 41(b) and 41(c), to a substantiallyexpanded (or fully opened) position as shown in FIG. 41(e). It should beappreciated that the flexible hinge 4118 allows the clamp 4100 to flex,twist, contort, expand, stretch, or flex in virtually any desired angleor position. For example, referring briefly to FIGS. 50(a)-50(d), theclamp 4100 is shown in a closed position in FIG. 50(a), opened such thatan angle α at the bight portion is less than 90° in FIG. 50(b), openedsuch that the angle α at the bight portion is approximately 180° in FIG.50(c), and opened such that the angle α at the bight portion is greaterthan 180° in FIG. 50(d).

Referring briefly to FIGS. 51(a)-51(c), the clamp 4100 is shown invarious contorted positions. As shown in FIGS. 51(a)-51(c), the flexiblehinge 4118 allows the clamp 4100 to twist, bend, and flex in virtuallyany desired angle or direction such that the first and second elongatedportions 4102 and 4104 may be displaced from each other at an angle (forexample, angle α) when viewing the clamp 4100 from an overview position,such as that provided in FIG. 51(a). In some embodiments, the flexiblehinge 4118 is stretchable and may twist to provide the first elongatedmember at a desired position in any of three orthogonal planes relativeto the second elongated member. In some embodiments, the flexibilityprovided by the hinge 4118 may be beneficial when positioning the firstand second elongated portions on the stomach during installation. Forexample, the flexible hinge 4118 allows the clamp 4100 to be installed,in one embodiment, into a smaller opening, such as an opening with atrocar, one elongated member at a time and then to properly install andposition the bariatric clamp 4100 on the stomach in the limited space ofthe abdominal cavity.

When the clamp 4100 is installed, the flexible hinge 4118 permitsexpansion and movement of the bight portion 4106 to accommodate anyirregularities in the stomach wall or fluctuations of thepassage-forming section. For example, FIG. 52(a) illustrates the clamp4100 in a closed position, wherein the flexible hinge 4118 is in acompressed, non-expanded position or resting state, and FIG. 52(b)illustrates the clamp 4100 in the closed position wherein the flexiblehinge 4118 is stretched or expanded in a tensioned state. As previouslymentioned, such stretching or expanding may accommodate irregularitiesin the stomach wall or fluctuations of the passage-forming section. Thestretching or expanding of the flexible hinge 4118 also allows the clamp4100 to accommodate variations in stomach thicknesses withoutcompromising the pressure applied by the clamp 4100, particularly in thepartition-forming section. In some embodiments, the flexible hinge 4118may be provided at a desired durometer or elasticity that may be thesame as or different from that of the polymer or silicone overmoldedportions provided in other areas of the clamp 4100, such as the firstand second elongated portions 4102 and 4104.

When installing the bariatric clamp 4100, the clamp 4100 is placed intoposition as explained in greater detail below, and the fastener portion4108 and engagement portion 4114 are used to retain the clamp 4100 in asubstantially closed position. FIGS. 41(b) and 41(c) illustrate theclamp 4100 in the substantially closed position. In the embodimentillustrated in FIGS. 41(a)-41(e), the fastener portion 4108 comprises astrap formed from the overmolded polymer, or other material, and locatedtowards the distal end of the second elongated portion 4104. Because thefastener portion 4108 is formed from the overmolded polymer in someembodiments, it is stretchable and capable of providing appropriatetension to partition the stomach when installed. Also, as shown in FIGS.53(a)-53(e), the fastener portion 4108 is capable of stretching so thatone of the primary openings 4110 may receive the engagement portion4114. The fastener portion 4108 may also include a secondary opening4112 used for adjusting or manipulating the fastener portion 4108, thesecond elongated portion 4104 and/or the clamp 4100. For example, asurgeon may use a tool (not shown) to engage the secondary opening 4112to position the strap such that the engagement portion 4114 engages oneof the primary openings 4110. In the embodiment illustrated in FIGS.41(a)-41(e) and 53(a)-53(e), the engagement portion 4114 comprises aprotrusion, such as a hook or tab, for engaging openings of the fastenerportion 4108.

In some embodiments, the clamp 4100 may be adjusted by disengaging theengagement portion 4114 from one of the primary openings 4110, andengaging the engagement portion 4114 with another one of the primaryopenings 4110 to either increase or decrease the spacing between thefirst and second elongated portions 4102 and 4104. In some embodiments,the fastener portion 4108 may be secured to the first elongated portion4102 by suturing the fastener portion 4108 to the polymer overmolding ofthe first elongated portion 4102.

FIGS. 42(a), 42(b), 43(a) and 43(b) illustrate embodiments of anovermolded bariatric clamp similar to that shown in FIGS. 41(a)-41(e)and described above, except that the embodiments illustrated in FIGS.42(a), 42(b), 43(a) and 43(b) have adjustable lengths. The adjustablelength of the bariatric clamp allows for the clamp to be furthercustomized to fit a patient's stomach during installation, or even afterthe clamp has been installed. For example, when installing the bariatricclamp, a surgeon is able to adjust the clamp as needed duringinstallation to fit the patient's stomach. Additionally, if a bariatricclamp having an adjustable length is installed in a patient, and thelength of the clamp is subsequently determined to be improper, thesurgeon is able to adjust the length of the clamp to better fit thepatient's stomach without having to remove the existing clamp or havingto install a new clamp. Accordingly, a bariatric clamp having anadjustable length may prevent unnecessary surgical operations and/orreduce the amount of time required to install or adjust the bariatricclamp.

One embodiment of a bariatric clamp 4200 having an adjustable length isillustrated in FIGS. 42(a) and 42(b). The clamp 4200 includes first andsecond adjustable substrate members 4201 and 4203 (shown dashed)overmolded in a polymer or elastomer material to form a first elongatedportion 4202, a second elongated portion 4204, a bight portion 4206, afastener portion 4208, and an engagement portion 4214. The first andsecond elongated portions 4202 and 4204 serve as a partition-formingsection of the bariatric clamp 4200. Referring briefly to FIGS. 42(a),42(b) and 10, when the clamp 4200 is installed within an abdominalcavity, the first and second elongated portions 4202 and 4204 areengaged to partition the stomach into a small, vertical pouch 500 and anexcluded section 502. The bight portion 4206 comprises a passage-formingsection located towards the proximal end of the clamp 4200. Thepassage-forming section allows gastric juices to flow 506 from theexcluded section 502 into the vertical pouch 500.

FIG. 42(a) illustrates the adjustable bariatric clamp 4200 in aretracted position wherein the length of the first elongated portion4202 and the length of the second elongated portion 4204 are decreasedto shorten the overall length of the clamp 4200. FIG. 42(b) illustratesthe adjustable bariatric clamp 4200 in an extended position wherein thefirst elongated portion 4202 and the second elongated portion 4204 areextended to increase the overall length of the clamp 4200. In theembodiment illustrated in FIGS. 42(a) and 42(b), the adjustable lengthis provided, at least in part, by the first and second adjustablesubstrate members 4201 and 4203 comprising the first and secondelongated portions 4202 and 4204, respectively, as well as portions ofthe bight portion 4206. As discussed herein, the adjustable substratemembers 4201 and 4203 are each referred to as a single member, but itshould be appreciated that they may each be comprised of two or morepieces as shown, for example, in FIGS. 42(a) and 42(b). It should alsobe appreciated that, in the embodiments discussed herein, the overmoldedmaterial is capable of stretching, expanding, and/or contracting toaccommodate the extended and retracted lengths of the first and secondelongated portions 4202 and 4204.

In some embodiments, the first adjustable substrate member 4201 maycomprise an external member 4201A and an internal member 4201B, whereinthe first adjustable substrate member 4201 is capable of at leastpartially disposing, or housing, the internal member 4201B within theexternal member 4201A. For example, the external member 4201A may beformed so that it has an opening 4205, or hollow portion, operable toreceive the internal member 4201B. In this embodiment, the length of thefirst elongated portion 4202 may be adjusted by extending or retractingthe internal member 4201B from or into the external member 4201A.Therefore, a user can extend the internal member 4201B from the externalmember 4201A as shown in FIG. 42(b) to increase the length of the firstelongated portion 4202. Conversely, the user can retract, or insert, theinternal member 4201B into the external member 4201A as shown in FIG.42(a) to decrease the length of the first elongated portion 4202. Insome embodiments, the external member 4201A, internal member 4201B, orboth may include one or more detents (not shown) or other means forretaining a particular length of the first elongated portion 4202.Additionally (or alternatively), the length of the first elongatedportion 4202 may be retained by suturing the first elongated portion4202 to a portion of the stomach, or to another device or tissue, toprevent unintentionally adjusting the length of the first elongatedportion 4202. In some embodiments, the length of the first elongatedportion 4202 may be further increased by fully extending or removing theinternal member 4201B from the external member 4201A. In otherembodiments, the first adjustable substrate member may comprise one ormore telescopic substrate members capable of telescopically expanding orretracting to adjust a length of the first elongated portion 4202 in amanner similar to that discussed above.

Similarly, in some embodiments, the second adjustable substrate member4203 may comprise an external member 4203A and an internal member 4203B,wherein the second adjustable substrate member 4203 is capable of atleast partially disposing, or housing, the internal member 4203B withinthe external member 4203A. For example, the external member 4203A may beformed so that it has an opening 4207, or hollow portion, operable toreceive the internal member 4203B. In this embodiment, the length of thesecond elongated portion 4204 may be adjusted by extending or retractingthe internal member 4203B from or into the external member 4203A.Therefore, a user can extend the internal member 4203B from the externalmember 4203A as shown in FIG. 42(b) to increase the length of the secondelongated portion 4204. Conversely, the user can retract, or insert, theinternal member 4203B into the external member 4203A as shown in FIG.42(a) to decrease the length of the second elongated portion 4204. Insome embodiments, the external member 4203A, internal member 4203B, orboth may include one or more detents (not shown) or other means forretaining a particular length of the second elongated portion 4204.Additionally (or alternatively), the length of the second elongatedportion 4204 may be retained by suturing the second elongated portion4204 to a portion of the stomach, or to another device or tissue, toprevent unintentionally adjusting the length of the second elongatedportion 4204. In some embodiments, the length of the second elongatedportion 4204 may be further increased by fully extending or removing theinternal member 4203B from the external member 4203A. In otherembodiments, the second adjustable substrate member may comprise one ormore telescopic substrate members capable of telescopically expanding orretracting to adjust a length of the second elongated portion 4204 in amanner similar to that discussed above.

As shown in FIGS. 42(a) and 42(b), the first and second elongatedportions 4202 and 4204 are joined by the bight portion 4206 at theproximal end of the clamp 4200. The bight portion 4206 includes aflexible hinge 4218 formed, in one implementation, from the polymerovermold. The flexible hinge 4218 allows the clamp 4200 to be positionedin a variety of positions ranging from a substantially closed position(similar to that illustrated in FIGS. 41(b) and 41(c)), to asubstantially expanded (or fully opened) position (similar to that shownin FIG. 41(e)). When the clamp 4200 is installed, the flexible hinge4218 permits expansion and movement of the bight portion 4206 toaccommodate any irregularities in the stomach wall or fluctuations ofthe passage-forming section. The flexible hinge 4218 also allows theclamp 4200 to accommodate variations in stomach thicknesses withoutcompromising the pressure applied by the clamp 4200, particularly in thepartition-forming section. In some embodiments, the flexible hinge 4218may be provided at a desired durometer or elasticity that may be thesame as or different from that of the polymer or silicone overmoldedportions provided in other areas of the clamp 4200, such as the firstand second elongated portions 4202 and 4204.

When installing the bariatric clamp 4200, the clamp 4200 is placed intoposition as explained in greater detail below, and the fastener portion4208 and engagement portion 4214 are used to retain the clamp 4200 in asubstantially closed position. In the embodiment illustrated in FIGS.42(a) and 42(b), the fastener portion 4208 comprises a strap formed fromthe overmolded polymer, or other material, and located towards thedistal end of the second elongated portion 4204. The strap may includeone or more primary openings 4210 for receiving the engagement portion4214, and a secondary opening 4212 used for adjusting or manipulatingthe fastener portion 4208, the second elongated portion 4204 and/or theclamp 4200. For example, a surgeon may use a tool (not shown) to engagethe secondary opening 4212 to position the strap such that theengagement portion 4214 engages one of the primary openings 4210. In theembodiment illustrated in FIGS. 42(a) and 42(b), the engagement portion4214 comprises a protrusion, such as a hook or tab, for engagingopenings of the fastener portion 4208.

In some embodiments, the clamp 4200 may be adjusted by disengaging theengagement portion 4214 from one of the primary openings 4210, andengaging the engagement portion 4214 with another one of the primaryopenings 4210 to either increase or decrease the spacing between thefirst and second elongated portions 4202 and 4204. In some embodiments,this adjustment of the clamp 4200 may also include adjusting the lengthof the clamp 4200 in accordance with the foregoing description. In someembodiments, the fastener portion 4208 may be secured to the firstelongated portion 4202 by suturing the fastener portion 4208 to thepolymer overmolding of the first elongated portion 4202.

Another embodiment of a bariatric clamp 4300 having an adjustable lengthis illustrated in FIGS. 43(a) and 43(b). The clamp 4300 includes firstand second substrate members 4301 and 4303 (shown dashed) and first andsecond bight substrate members 4305 and 4307 (shown dashed) overmoldedin a polymer or elastomer material to form a first elongated portion4302, a second elongated portion 4304, a bight portion 4306, a fastenerportion 4308, and an engagement portion 4314. The first and secondelongated portions 4302 and 4304 serve as a partition-forming section ofthe bariatric clamp 4300. Referring briefly to FIGS. 43(a), 43(b) and10, when the clamp 4300 is installed within an abdominal cavity, thefirst and second elongated portions 4302 and 4304 are engaged topartition the stomach into a small, vertical pouch 500 and an excludedsection 502. The bight portion 4306 comprises a passage-forming sectionlocated towards the proximal end of the clamp 4300. The passage-formingsection allows gastric juices to flow 506 from the excluded section 502into the vertical pouch 500.

FIG. 43(a) illustrates the adjustable bariatric clamp 4300 in aretracted position wherein the length of the first elongated portion4302 and the length of the second elongated portion 4304 are decreasedto shorten the overall length of the clamp 4300. FIG. 43(b) illustratesthe adjustable bariatric clamp 4300 in an extended position wherein thefirst elongated portion 4302 and the second elongated portion 4304 areextended to increase the overall length of the clamp 4300. In theembodiment illustrated in FIGS. 43(a) and 43(b), the adjustable lengthis provided, at least in part, by a first adjustable portion 4302Aformed from the polymer overmold comprising the first elongated portion4302 and a second adjustable portion 4304A formed from the polymerovermold comprising the second elongated portion 4304. The first andsecond adjustable portions 4302A and 4304A are shown in a retractedposition in FIG. 43(a), and in an extended position in FIG. 43(b). Itshould be appreciated that, in some embodiments, the first and secondadjustable portions 4302A and 4304A may be comprised of a materialdifferent from the polymer overmolding.

In some embodiments, the first adjustable portion 4302A is capable ofextending (e.g., stretching, expanding, etc.) to increase the length ofthe first elongated portion 4302 and retracting (e.g., contracting) todecrease the length of the first elongated portion 4302. Therefore, auser may adjust the length of the first elongated portion 4302 byadjusting the position or placement of the first elongated portion 4302,while the first adjustable portion 4302A extends or retracts accordinglyto account for corresponding adjustments of the length of the firstelongated portion 4302. Similarly, in some embodiments, the secondadjustable portion 4304A is capable of extending (e.g., stretching,expanding, etc.) to increase the length of the second elongated portion4304 and retracting (e.g., contracting) to decrease the length of thesecond elongated portion 4304. Therefore, a user may adjust the lengthof the second elongated portion 4304 by adjusting the position orplacement of the second elongated portion 4304, while the secondadjustable portion 4304A extends or retracts accordingly to account forcorresponding adjustments of the length of the second elongated portion4304.

As discussed herein, the first and second adjustable portions 4302A and4304A are capable of stretching, expanding, and/or contracting toaccommodate the extended and retracted lengths of the first and secondelongated portions 4302 and 4304. In some embodiments, the length of thefirst and/or second elongated portions 4302 and 4304 may be retained bysuturing the first and/or second elongated portions 4302 and 4304 to aportion of the stomach, or to another device or tissue, to preventunintentionally adjusting the length of the first and/or secondelongated portions 4302 and 4304. Although FIGS. 43(a) and 43(b)illustrate the first adjustable portion 4302A disposed at a locationadjacent the first bight substrate member 4305 and the first substratemember 4301, the first adjustable portion 4302A may be disposed at otherlocations along the length of the first elongated portion 4302.Similarly, although FIGS. 43(a) and 43(b) illustrate the secondadjustable portion 4304A disposed at a location adjacent the secondbight substrate member 4307 and the second substrate member 4303, thesecond adjustable portion 4304A may be disposed at other locations alongthe length of the second elongated portion 4304.

In some embodiments, the first and second adjustable portions 4302A and4304A are capable of bending, flexing or hinging such that the bightportion 4306 is capable of being disposed at a desired angle relative tothe length of the first and second elongated portions 4302 and 4304. Forexample, FIG. 54(a) illustrates an embodiment wherein the clamp 4300 isinstalled on a stomach 5400 and the first and second adjustable portions4302A and 4304A are hinged such that the bight portion 4306 is angled ina first direction relative to the first and second elongated portions4302 and 4304. In another example embodiment, FIG. 54(b) illustrates theclamp 4300 installed on the stomach 5400 and the first and secondadjustable portions 4302A and 4304A are hinged such that the bightportion 4306 is angled in a second direction relative to the first andsecond elongated portions 4302 and 4304. In some embodiments, thehinging portion of the clamp 4300 as described herein may be provided byhinges or other features incorporated in the clamp 4300 at locationswhere the first and second elongated portions 4302 and 4304 join thebight portion 4306. In some embodiments, the first and second adjustableportions 4302A and 4304A may maintain the bight portion 4306 at a fixedangle.

It should be appreciated that, in some embodiments, the clamp may bepositioned at various locations along the stomach as desired. Forexample, as shown in FIG. 54(a), the top portion of the clamp may bepositioned at a location at the top of the stomach adjacent theesophagus and the bottom portion of the clamp may be positioned at alocation at the bottom of the stomach horizontally off-set relative tothe location at which the top portion of the clamp is positioned. Thismay be achieved by providing a clamp that can bend, flex, adjust, hinge,or curve to achieve the desired positioning (as is the case in FIG.54(a)), or it may be achieved by positioning the clamp so that it isangled with respect to a vertical axis extending from the bottom of thestomach towards the top of the stomach. In some embodiments, suchpositioning may be useful for ensuring that the vertical food pouch orthe portion of the stomach beneath the esophagus has a substantiallyuniform size from the top of the stomach towards the bottom portion ofthe stomach.

As shown in FIGS. 43(a) and 43(b), the first and second elongatedportions 4302 and 4304 are joined by the bight portion 4306 at theproximal end of the clamp 4300. The bight portion 4306 includes a firstbight substrate member 4305, second bight substrate member 4307, and aflexible hinge 4318 formed, in one implementation, from the polymerovermold. The first and second bight substrate members 4305 and 4307 aresimilar (in both functionality and composition) to the first and secondsubstrate members 4301 and 4303 (and other substrate members disclosedherein), and may be formed of various biocompatible materials such astitanium or biocompatible polymer resins such as polyether ketone ketone(PEKK) or polyether ether ketone (PEEK). The flexible hinge 4318 allowsthe clamp 4300 to be positioned in a variety of positions ranging from asubstantially closed position (similar to that illustrated in FIGS.41(b) and 41(c)), to a substantially expanded (or fully opened) position(similar to that shown in FIG. 41(e)). When the clamp 4300 is installed,the first and second bight substrate members 4305 and 4307 providestructural support to the passage-forming section of the clamp 4300.Additionally, the flexible hinge 4318 permits expansion and movement ofthe bight portion 4306 to accommodate any irregularities in the stomachwall or fluctuations of the passage-forming section. The flexible hinge4318 also allows the clamp 4300 to accommodate variations in stomachthicknesses without compromising the pressure applied by the clamp 4300,particularly in the partition-forming section. In some embodiments, theflexible hinge 4318 may be provided at a desired durometer or elasticitythat may be the same as or different from that of the polymer orsilicone overmolded portions provided in other areas of the clamp 4300,such as the first and second elongated portions 4302 and 4304.

When installing the surgical clamp 4300, the clamp 4300 is placed intoposition as explained in greater detail below, and the fastener portion4308 and engagement portion 4314 are used to retain the clamp 4300 in asubstantially closed position. In the embodiment illustrated in FIGS.43(a) and 43(b), the fastener portion 4308 comprises a strap formed fromthe overmolded polymer, or other material, and located towards thedistal end of the second elongated portion 4304. The strap may includeone or more primary openings 4310 for receiving the engagement portion4314, and a secondary opening 4312 used for adjusting or manipulatingthe fastener portion 4308, the second elongated portion 4304 and/or theclamp 4300. For example, a surgeon may use a tool (not shown) to engagethe secondary opening 4312 to position the strap such that theengagement portion 4314 engages one of the primary openings 4310. In theembodiment illustrated in FIGS. 43(a) and 43(b), the engagement portion4314 comprises a protrusion, such as a hook or tab, for engagingopenings of the fastener portion 4308.

In some embodiments, the clamp 4300 may be adjusted by disengaging theengagement portion 4314 from one of the primary openings 4310, andengaging the engagement portion 4314 with another one of the primaryopenings 4310 to either increase or decrease the spacing between thefirst and second elongated portions 4302 and 4304. In some embodiments,this adjustment of the clamp 4300 may also include adjusting the lengthof the clamp 4300 in accordance with the foregoing description. In someembodiments, the fastener portion 4308 may be secured to the firstelongated portion 4302 by suturing the fastener portion 4308 to thepolymer overmolding of the first elongated portion 4302.

FIGS. 44(a) and 44(b) illustrate yet another embodiment of a bariatricclamp 4400 having an adjustable length. The bariatric clamp 4400 variesfrom the bariatric clamps discussed above with respect to FIGS.41(a)-41(e), 42(a), 42(b), 43(a) and 43(b) in that the bariatric clamp4400 in FIGS. 44(a) and 44(b) is comprised of multiple members, ratherthan a continuous design. However, it should be appreciated that theclamp 4400 operates in a manner similar to those discussed above.

The bariatric clamp 4400 includes a first substrate member 4401, secondsubstrate member 4403, first bight substrate member 4405 and secondbight substrate member 4407 (each shown dashed). The first substratemember 4401 is overmolded in a polymer material to form a firstelongated member 4402 having an engagement portion 4414 at a distal endand a first receiving portion 4416 towards a proximal end of the firstelongated member 4402. The second substrate member 4403 is overmolded ina polymer material to form a second elongated member 4404 having afastener portion 4408 at a distal end and a second receiving portion4417 at a proximal end of the second elongated member 4404. The firstand second bight substrate members 4405 and 4407 are overmolded in apolymer material to form a bight member 4406 having a flexible hinge4418, first retention feature 4420 and second retention feature 4422.When the clamp 4400 is assembled, the first retention feature 4420 isreceived by the first receiving portion 4416 to couple the bight member4406 to the first elongated member 4402, and the second retentionfeature 4422 is received by the second receiving portion 4417 to couplethe bight member 4406 to the second elongated member 4404. The bightmember 4406 comprises a passage-forming section disposed towards aproximal end of the clamp 4400, and the first and second elongatedmembers 4402 and 4404 comprise a partition-forming section disposedtowards a distal end of the clamp 4400.

Referring briefly to FIGS. 44(a), 44(b) and 10, when the clamp 4400 isinstalled within an abdominal cavity, the first and second elongatedmembers 4402 and 4404 are engaged to partition the stomach into a small,vertical pouch 500 and excluded section 502. The bight member 4406comprises the passage-forming section located towards the proximal endof the clamp 4400 and allows gastric juices to flow 506 from theexcluded section 502 into the vertical pouch 500.

In the embodiment illustrated in FIGS. 44(a) and 44(b), the adjustablelength is provided, at least in part, by the positions of the first andsecond retention features 4420 and 4422 with respect to the receivingportions 4416 and 4417 of the first and second elongated members,respectively. For example, FIG. 44(a) illustrates the adjustablebariatric clamp 4400 in a retracted position wherein the first andsecond retention features 4420 and 4422 are positioned so that theoverall length of the clamp 4400 is decreased. FIG. 44(b) illustratesthe adjustable bariatric clamp 4400 in an extended position wherein thefirst and second retention features 4420 and 4422 are positioned so thatthe overall length of the clamp 4400 is increased.

In some embodiments such as, for example, that illustrated in FIGS.44(a) and 44(b), the first retention feature 4420 and the secondretention feature 4422 each comprise a ratchet feature having aplurality of teeth 4424 formed from the polymer overmold material, andthe receiving portions 4416 and 4417 each comprise a loop-type shapeformed from the polymer overmold material. The teeth 4424 are capable offlexing to fit within the opening of the loop when the retention feature4420/4422 is inserted into the receiving portion 4416/4417. This allowsthe retention feature 4420/4422 to slide through the opening of thereceiving portion 4416/4417 to couple the bight member 4406 to therespective first or second elongated member 4402 or 4404. Once a tooth4424 of the retention feature 4422/4424 has passed through the receivingportion 4416/4417, the tooth 4424 is capable of engaging the receivingportion 4416/4417 to prevent the retention feature 4422/4424 fromunintentionally disengaging from the receiving portion 4416/4417.However, if a user wishes to remove at least a portion of the retentionfeature 4420/4422 from the receiving portion 4416/4417 (for example, tolengthen or disassemble the clamp 4400), the user may flex, or stretch,the receiving portion 4416/4417 and/or compress the tooth 4424 towithdraw the retention feature 4420/4422 from the respective receivingportion 4416/4417.

As mentioned above, the adjustable length of the clamp 4400 is provided,at least in part, by the positions of the first and second retentionfeatures 4420 and 4422 with respect to the receiving portions 4416 and4417 of the first and second elongated members, respectively. Todecrease the length of the clamp 4400, the user may insert the firstand/or second retention features 4420 and 4422 into the respectivereceiving portions 4416 and 4417 as discussed above. If a user wishes tofurther decrease the length of the clamp 4400, the user can furtherinsert the first and/or second retention features 4420 and 4422 into therespective receiving portions 4416 and 4417 so that additional teeth4424 have passed through the receiving portions 4416 and 4417. Forexample, FIG. 44(a) shows the clamp 4400 in its most retracted, orshortest, position. In this embodiment, all teeth 4424 of the first andsecond retention features 4420 and 4422 have passed through theirrespective receiving portions 4416 and 4417. To increase the length ofthe clamp 4400, the user may remove a portion of the first and/or secondretention features 4420 and 4422 from their respective receivingportions 4416 and 4417 as discussed above. If the user wishes to furtherincrease the length of the clamp 4400, the user can further remove aportion of the first and/or second retention features 4420 and 4422 fromthe respective receiving portions 4416 and 4417 so that additional teeth4424 have passed back through the receiving portions 4416 and 4417. Forexample, FIG. 44(b) illustrates the clamp 4400 in its most extended, orlongest, assembled position. In this embodiment, all teeth 4424 havebeen withdrawn from the receiving portions 4416 and 4417 except for thelast tooth 4424 of each retention feature 4420 and 4422 that maintainsthe coupling between the bight member 4406 and the first and secondelongated members 4402 and 4404.

As shown in FIGS. 44(a) and 44(b), the first and second elongatedmembers 4402 and 4404 are coupled to the bight member 4406 towards theproximal end of the clamp 4400. As discussed above, the bight member4406 includes the first and second bight substrate members 4405 and4407, the first and second retention features 4420 and 4422, and aflexible hinge 4418 formed, in one implementation, from the polymerovermold. The first and second bight substrate members 4405 and 4407 aresimilar (in both functionality and composition) to the first and secondsubstrate members 4401 and 4403 (and other bight substrate membersdisclosed herein), and may be formed of various biocompatible materialssuch as titanium or biocompatible polymer resins such as polyetherketone ketone (PEKK) or polyether ether ketone (PEEK). The flexiblehinge 4418 allows the assembled clamp 4400 to be positioned in a varietyof positions ranging from a substantially closed position (similar tothat illustrated in FIGS. 41(b) and 41(c)), to a substantially expanded(or fully opened) position (similar to that shown in FIG. 41(e)). Whenthe clamp 4400 is installed, the first and second bight substratemembers 4405 and 4407 provide structural support to the passage-formingsection of the clamp 4400. Additionally, the flexible hinge 4418 permitsexpansion and movement of the bight member 4406 to accommodate anyirregularities in the stomach wall or fluctuations of thepassage-forming section. The flexible hinge 4418 also allows the clamp4400 to accommodate variations in stomach thicknesses withoutcompromising the pressure applied by the clamp 4400, particularly in thepartition-forming section. In some embodiments, the flexible hinge 4418may be provided at a desired durometer or elasticity that may be thesame as or different from that of the polymer or silicone overmoldedportions provided in other areas of the clamp 4400, such as the firstand second elongated members 4402 and 4404.

When installing the assembled bariatric clamp 4400, the clamp 4400 isplaced into position as explained in greater detail below, and thefastener portion 4408 and engagement portion 4414 are used to retain theclamp 4400 in a substantially closed position. In the embodimentillustrated in FIGS. 44(a) and 44(b), the fastener portion 4408comprises a strap formed from the overmolded polymer, or other material,and located towards the distal end of the second elongated member 4404.The strap may include one or more primary openings 4410 for receivingthe engagement portion 4414, and a secondary opening 4412 used foradjusting or manipulating the fastener portion 4408, the secondelongated member 4404 and/or the clamp 4400. For example, a surgeon mayuse a tool (not shown) to engage the secondary opening 4412 to positionthe strap such that the engagement portion 4414 engages one of theprimary openings 4410. In the embodiment illustrated in FIGS. 44(a) and44(b), the engagement portion 4414 comprises a protrusion, such as ahook or tab, for engaging openings of the fastener portion 4408.

In some embodiments, the assembled clamp 4400 may be adjusted bydisengaging the engagement portion 4414 from one of the primary openings4410, and engaging the engagement portion 4414 with another one of theprimary openings 4410 to either increase or decrease the spacing betweenthe first and second elongated members 4402 and 4404. In someembodiments, this adjustment of the clamp 4400 may also includeadjusting the length of the clamp 4400 in accordance with the foregoingdescription. In some embodiments, the fastener portion 4408 may besecured to the first elongated member 4402 by suturing the fastenerportion 4408 to the polymer overmolding of the first elongated member4402.

FIG. 45 illustrates a flow diagram 4500 illustrating a method forinstalling a bariatric clamp. For the sake of clarity, the methodillustrated in FIG. 45 is generally discussed with reference to thebariatric clamp 4100 illustrated in FIGS. 41(a)-41(e) and describedabove, unless otherwise specified. However, it should be appreciatedthat the disclosed method for installing a bariatric clamp may beapplicable to various embodiments of a bariatric clamp including, butnot limited to, any of the embodiments discussed herein, and any of theembodiments discussed above with respect to FIGS. 41-44. Additionally,when describing the method presented in FIG. 45 (and the methodpresented in FIG. 47), it should be understood that references to the“first elongated portion” and “second elongated portion” are not limitedto the exact embodiments of a “first elongated portion” and “secondelongated portion” as illustrated in any of the figures described above.For example, as used in the context of the methods discussed withreference to FIGS. 45 and 47, the “first elongated portion” of FIG. 41may refer to a first half of the bariatric clamp 4100 including thefirst elongated portion 4102, the engagement portion 4114, and thesection of the bight portion 4106 located on the same side of thebariatric clamp 4100. Similarly, the “second elongated portion” mayrefer to a second half of the bariatric clamp 4100 including the secondelongated portion 4104, the fastener portion 4108, and the section ofthe bight portion 4106 located on the same side of the bariatric clamp4100. It should also be noted that, in some embodiments, the firstelongated portion may include the fastener portion, whereas the secondelongated portion includes the engagement portion.

The method of FIG. 45 first discloses, at block 4502, creating anopening in the abdominal cavity of a patient to allow access to thepatient's stomach. In some embodiments, this may include inserting oneor more trocars into the patient's abdomen, wherein the trocars providean opening through which a surgeon may insert various devices andequipment such as, for example, surgical tools, a camera and thebariatric clamp 4100. The trocars may comprise various features known inthe art. For example, one or more of the trocars may, in someembodiments, include a cutting portion to assist the surgeon (or otherpersonnel) with penetrating the abdominal cavity (or other tissue) ofthe patient. In some embodiments, other tools (e.g., scissors, needles,dilators, etc.) may be used to create the opening in the abdominalcavity so that the trocar can be inserted into the abdominal cavity. Insome embodiments, the abdominal cavity may be inflated by forcing air(e.g., CO2) into the abdominal cavity. In such embodiments, a hose ortube may be inserted into or connected to one or more of the trocars,and the trocars may include a seal to prevent the air from escaping theabdominal cavity through the trocars. In some embodiments, a camera orendoscope may be placed into the abdominal cavity to allow a surgeon orother personnel to view installation, removal or adjustment of thebariatric clamp 4100. In such embodiments, the endoscope may be placedinto the abdominal cavity through a trocar inserted, for example, at thenavel of the patient.

At block 4504, the method discloses removing tissue connected to thestomach, particularly at locations where the bariatric clamp 4100 is tobe positioned adjacent the stomach. Tissue attached to or adhered to theexterior surface of the stomach is removed to create a tunnel, path orpassageway on the exterior surface of the stomach for the first andsecond elongated portions 4102 and 4104 of the bariatric clamp 4100 toreside on the stomach, such as in a vertical orientation, or primarilyvertical orientation, on the anterior and posterior sides of theexterior surfaces of the stomach, to partition the stomach, as describedherein, and while providing a passage-forming section to allow some flowor exchange of gastric fluids between the first and second regions. Whenthe bariatric clamp 4100 is in a closed position, some gastric juicesare believed likely to be exchanged across both the first and secondregions, and primarily through the passage forming section of thebariatric clamp 4100.

In some embodiments, the removal of the tissue may be accomplished byresecting the tissue using surgical equipment such as, for example,clamps, forceps, vacuum hoses, scalpels, an ultrasonic probe, or anycombination thereof to create a passageway, tunnel or path for thebariatric clamp 4100 or any other surgical tools (e.g., alignmentdevice, guide member, etc.) used in the installation process.Additionally, this step may include displacing tissue and/or organs(e.g., the liver) located towards a top, bottom, anterior and/orposterior side of the stomach to expose the stomach to provide easieraccess to the stomach. This may also include exposing one or morelocations where the bariatric clamp 4100, or other surgical equipment ortools, can be positioned onto the stomach with little or no interveningtissue.

At block 4506, the method discloses positioning the bariatric clamp 4100in a substantially expanded or opened position. Referring briefly toFIGS. 46 and 50(a)-50(d), the bariatric clamp 4100 of FIGS. 41(a)-41(e)is illustrated in various opened positions (FIG. 41(e) also illustratesthe bariatric clamp 4100 in a substantially expanded or openedposition). As shown in FIG. 46, the clamp 4100 is placed in an openedposition such that the bariatric clamp 4100 is capable of fitting intothe opening of the abdominal cavity of the patent in the opened positionwherein the first and second elongated portions 4102 and 4104 separatelypass through the opening in the abdominal cavity. In some embodiments,this may include fitting the opened bariatric clamp 4100 through atrocar (e.g., a 12 mm trocar) while the bariatric clamp 4100 is in anopened or substantially expanded position. It should be appreciated thatthe fastener portion 4108 is comprised of the polymer overmolding, andis therefore capable of flexing, as shown in FIG. 46, to fit within theopening of the abdominal cavity. Similarly, the flexible hinge 4118 isalso comprised of the polymer overmolding, and is also capable offlexing to allow the first and second elongated portions to contort oradjust while the bariatric clamp 4100 is inserted into the opening ofthe abdominal cavity. In some embodiments, positioning the bariatricclamp 4100 in the expanded position may include aligning the first andsecond elongated portions such that a length 11 of the first elongatedportion 4102 is substantially collinear with a length 12 of the secondelongated portion 4104. In some embodiments, positioning the clamp inthe expanded position may include assembling the clamp, for example, ifthe embodiment of the clamp 4400 provided in FIGS. 44(a) and 44(b) isimplemented. However, in alternate embodiments, the clamp 4400 in FIGS.44(a) and 44(b) may be assembled after being inserted into the abdominalcavity.

At block 4508 of FIG. 45, the bariatric clamp 4100 is inserted into theabdominal cavity in the substantially expanded or opened positiondiscussed herein. FIG. 47 provides a flow diagram 4700 illustrating oneembodiment of a method for inserting the bariatric clamp 4100 into theabdominal cavity in the opened position. The method illustrated in FIG.47 implements an alignment device (e.g., Gold finger, clamp, forceps,etc.) to position a guide member (e.g., suture, string, thread, twine,wire, etc.), wherein the guide member is used to guide the bariatricclamp 4100 as it is inserted into the abdominal cavity and/or positionedadjacent the stomach. While describing the method of FIG. 47, referenceis made to FIGS. 48(a) and 48(b), which illustrate various views of thepatient's stomach 4800. FIG. 48(a) illustrates an overview perspectiveof a first side 4810, top 4815 and bottom 4817 of the patient's stomach4800. FIG. 48(b) illustrates a profile view of the stomach 4800 asviewed along line A-A in FIG. 48(a). The profile view shows the firstside 4810, top 4815 and bottom 4817 of the stomach 4800 and a secondside 4820 of the stomach 4800. In some embodiments, the first side 4810may be the posterior side of the stomach and the second side 4820 may bethe anterior side of the stomach, however in other embodiments, thefirst side 4810 may be the anterior side of the stomach and the secondside 4820 may be the posterior side of the stomach.

Referring briefly to FIGS. 49(a) and 49(b), an example embodiment of analignment device, or tool 4900 is shown having an end member 4910disposed at a distal end of the tool 4900, and a handle 4920 disposed ata proximal end of the tool 4900. The end member 4910 is disposed at theend of a shaft portion 4915 of the tool 4900 and, in some embodiments,includes an opening 4912 for receiving and/or retaining a guide member(e.g., suture). As explained in greater detail below, the tool 4900 maybe used to assist with positioning the guide member through a tunnel orpath created along a side of the stomach and around the top of thestomach. In some embodiments, the end member 4910 may be articulated inan upward direction with reference to the horizontal shaft portion 4915as shown in FIG. 49(a), and may also be articulated to be positionedin-line with the shaft portion 4915 as shown in FIG. 49(b). Articulationof the end member 4910 may be controlled by actuating the handle 4920 asshown in FIGS. 49(a) and 49(b).

In the method of FIG. 47, the alignment device is used to position theguide member so that it may be used to guide the bariatric clamp 4100into the abdominal cavity, and into position as further described below.At block 4702, a first end of the guide member is attached to a distalend of the alignment device (or the first end of the guide member isgrasped using the distal end of the alignment device), and the alignmentdevice is inserted into the abdominal cavity (e.g., through a trocar).At block 4704, the alignment device is positioned along the first side4810 of the stomach 4800 by traversing the distal end of the alignmentdevice along the first side 4810 of the stomach towards the top 4815 ofthe stomach 4800. Once positioned at the top 4815 of the stomach 4800(e.g., at location 4805), the distal end of the alignment device (e.g.,the end member 4910 of tool 4900) is positioned (e.g., articulated,extended, etc.) so that a portion of the guide member is accessible fromthe second side 4820 of the stomach 4800, while the a portion of thealignment device (e.g., the shaft portion 4915 of tool 4900) remainspositioned along the first side 4810 of the stomach 4800. At block 4706,the guide member is then positioned on the second side 4820 of thestomach 4800 (for example, using a clamp or forceps), while the firstend of the guide member remains attached to the distal end of thealignment device (e.g., the end member 4910 of tool 4900).

At block 4708, the alignment device is withdrawn from the first side4810 of the stomach 4800 (and preferably withdrawn from the abdominalcavity) by traversing the first side 4810 of the stomach in a directiontowards the bottom 4817 of the stomach 4800 such that a first portion4825A of the guide member is positioned or aligned along the first side4810 of the stomach 4800, while a second portion 4825B of the guidemember is retained (for example, using a clamp or forceps) on the secondside 4820 of the stomach 4800. FIGS. 48(a) and 48(b) illustrate thefirst portion of the guide member 4825A and the second portion of theguide member 4825B, in accordance with the present embodiment. In thisembodiment, the first portion of the guide member is aligned such thatthe position of the first portion of the guide member is relativelyconsistent with the location at which an elongated portion 4102/4104 ofthe clamp 4100 will be positioned adjacent the first side 4810 of thestomach 4800.

At block 4710, the first end of the guide member is then disconnectedfrom the alignment device and attached to one of the first or secondelongated portions 4102 or 4104 of the bariatric clamp 4100. In someembodiments, this may be accomplished by attaching the guide memberthrough the secondary opening 4112 and/or around the fastener portion4108 of the second elongated portion 4104 of the clamp 4100. In otherembodiments, this may be accomplished by attaching the guide member tothe engagement portion 4114 of the first elongated portion 4102. Atblock 4712, with the first end of the guide member attached to eitherthe first elongated portion 4102 or the second elongated portion 4104,and the clamp 4100 positioned in the substantially expanded position,the second portion of the guide member 4825B is engaged to guide thebariatric clamp 4100 into the abdominal cavity. In some embodiments,this may be accomplished by pulling on the second portion of the guidemember with surgical tools (e.g., forceps, clamps, etc.) to extract thefirst portion of the guide member 4825A from the first side 4810 of thestomach 4800 while feeding the bariatric clamp 4100 into a trocar whilethe clamp 4100 remains in the substantially expanded position.

Referring again to FIG. 45, the first or second elongated portion4102/4104 of the clamp 4100 attached to the guide member at block 4710is then positioned adjacent the first side 4810 of the stomach 4800 atblock 4510, while the clamp 4100 remains in an opened position. In someembodiments, this may be accomplished by continuing to engage the secondportion of the guide member 4825B until the respective first or secondelongated portion 4102 or 4104 is positioned adjacent the first side4810 of the stomach. At this time, the guide member may be disconnectedfrom the first or second elongated portion 4102 or 4104 and removed fromthe abdominal cavity. Additionally, other surgical tools (e.g., clamps,forceps, scissors, etc.) may be used to position the first or secondelongated portion 4102 or 4104 adjacent the first side 4810 of thestomach 4800.

The remaining elongated portion is then positioned adjacent the secondside 4820 of the stomach 4800 at block 4512. The clamp 4100 should bepositioned so that the bight portion 4106 of the clamp 4100 is abuttingthe bottom 4817 of the stomach 4800. In some embodiments, surgical toolsmay be used to engage the remaining elongated portion and to properlyposition the elongated portion adjacent the second side 4820 of thestomach 4800. Although the method is described in accordance with apreferred embodiment, it should be understood that, in some embodiments,the clamp 4100 may be installed in a sequence wherein blocks 4510 and4512 are performed in reversed order.

At block 4514, the bariatric clamp 4100 is closed to partition thestomach in accordance with the disclosure provided above with respect tothe various embodiments of the bariatric (or surgical) clamps. In someembodiments, this may include stretching the tissue of the stomach alongthe length of the clamp 4100 to eliminate folds in the stomach tissue.In some embodiments, closing the clamp 4100 may also include securingthe clamp 4100 in the closed position. For example, closing and securingthe bariatric clamp 4100 of FIG. 41(a) may include using a tool toengage the fastener portion 4108 (for example, at the secondary opening4112) to position the fastener portion 4108 such that the engagementportion 4114 engages one of the primary openings 4110.

In some embodiments, closing the bariatric clamp 4100 may also includeaffixing the first elongated portion 4102 to the side of the stomachadjacent the first elongated portion 4102, and/or affixing the secondelongated portion 4104 to the side of the stomach adjacent the secondelongated portion 4104 to prevent unwanted migration or displacement ofportions of the clamp 4100. In some embodiments, this may beaccomplished by suturing the first and second elongated portions 4102and 4104 to their respective sides of the stomach. For example, thefirst elongated portion 4102 may be sutured to the first side of thestomach (assuming the clamp 4100 is installed such that the first sideof the stomach is adjacent the first elongated portion 4102) by suturingthrough the overmolded portion of the first elongated portion 4102.Similarly, the second elongated portion 4104 may be sutured to thesecond side of the stomach (assuming the clamp 4100 is installed suchthat the second side of the stomach is adjacent the second elongatedportion 4104) by suturing through the overmolded portion of the secondelongated portion 4104.

An example of one such embodiment is illustrated in FIG. 55, whichillustrates a clamp 5500, similar to the clamp 4100 discussed herein,having curved suturing needles 5502 embedded or encapsulated within thepolymer overmolding of the bariatric clamp 5500 and used to anchor thefirst elongated portion 5508 and/or second elongated portion 5510 to thestomach once the clamp 5500 is properly installed and positioned. Insome embodiments, the substrate members (e.g., first substrate member5504) may be modified to accommodate the placement of the suturingneedles 5502. For example, as shown in FIG. 55, the first substratemember 5504 and second substrate member 5512 include various recesses5506 to accommodate placement of the suturing needles. In someembodiments, a clamp modified such as that shown in FIG. 55 may beinserted into the abdominal cavity of the patient having the curvedsuturing needles 5502 embedded or encapsulated within the polymerovermolding of the bariatric clamp and having sutures 5514 coupled tothe curved suturing needles 5502. In such an embodiment, once the firstand/or second elongated portions 5508 and/or 5510 are properlypositioned, pressure may be applied to the needles 5502 or elongatedportion of the clamp such that the needles 5502 protrude from thepolymer overmolding and into the adjacent walls of the stomach to suturethe respective first and/or second elongated portions 5508 and/or 5510to the stomach. In some embodiments, the suture needles 5502 may bemanipulated using the suture(s) 5514 attached to the respective needle5502. In some embodiments, instead of applying pressure to the needles5502 as discussed above, the needles 5502 may be extracted from thepolymer overmolding by manipulating the needles 5502 with the attachedsuture(s) 5514. Referring briefly to FIG. 46, the clamp may, in someembodiments, include one or more visual indicators 4602 for defininglocations where sutures may be applied to or embedded within the clamp.

In some embodiments, the bariatric clamp may be attached to andpositioned on the exterior surface of the patient's stomach using one ormore toggle suture assemblies that are either partially or fullypositioned from the exterior of the stomach to the stomach wall or fromthe exterior wall of the stomach to the interior of the stomach,depending on a desired implementation of a toggle suture. For example,the embodiment of the clamp 5500 illustrated in FIG. 55 may be modifiedsuch that the curved needles 5502 in FIG. 55 are replaced by a togglesuture or toggle suture assembly (such as a toggle suture assembly knownin the art). In some embodiments, one or more toggle suture assembliesmay be temporarily inserted into the clamp 5500 at various locations(e.g., at the recesses 5506) or, in other embodiments, may be lockmolded, machined, or installed at desired locations on the bariatricclamp to assist with installation of the clamp on the patient's stomach.In some embodiments, the toggle suture assemblies can be retroactivelyinstalled in a pre-manufactured clamp 5500. In one embodiment, varioustoggle suture assemblies are provided adjacent the first and second endsof the bariatric clamp, such as adjacent the flexible hinge and/or theconnection point where the bariatric clamp is closed, and along thefirst and second elongated members and the bight portion, as desired.

It should be appreciated that the bariatric clamp and/or sutures may beimplemented using known or available absorbable materials, such asbio-absorbable materials (e.g., catgut suture), that provide desirableor suitable mechanical or structural properties and integrity for adesired or needed period of time prior to being absorbed ordisintegrating to an unacceptable level. Either natural or syntheticallyabsorbable materials may be used. Poly glycol, for example, may be usedin certain implementations.

In some embodiments, the method illustrated in FIG. 45 may furtherinclude adjusting a length of the bariatric clamp as discussed abovewith respect to the clamps illustrated in FIGS. 42(a), 42(b), 43(a),43(b), 44(a) and 44(b). Depending upon the particular embodiment of theclamp, the length of the bariatric clamp may be adjusted in a variety ofways. For example, in the embodiments discussed above with respect toFIGS. 42(a), 42(b), 43(a) and 43(b), the length of the clamp may beadjusted by adjusting the length of the first elongated portion and/orthe second elongated portion. In the embodiments discussed above withrespect to FIGS. 44(a) and 44(b), the length of the clamp may beadjusted by adjusting the positions of the first and second retentionfeatures with respect to the receiving portions of the first and secondelongated members. Regardless of which clamp is used, the length may beadjusted at any point during the clamp installation. However, it ispreferable to adjust the length of the clamp prior to securing the clampto the patient's stomach. Nevertheless, the clamp may also beuninstalled by reversing any of the steps discussed above (e.g., byremoving sutures affixing any portions of the clamp to the stomach), sothat the clamp may be removed or adjusted, wherein such adjustments mayinclude adjusting the length of the clamp as discussed herein, oradjusting a position of the clamp on the stomach.

In some embodiments, the method for installing a bariatric clamp mayfurther include ensuring proper installation of the bariatric clamp4100. This may include measuring a pressure applied on the stomach bythe clamp 4100. In some embodiments, the pressure may be measured byplacing one or more pressure transducers between the clamp 4100 and oneof the sides of the stomach. In some embodiments, a pressure in therange of 0-2 or 0-3 inHg may be desired. Additionally, ensuring properinstallation may, in some embodiments, include inserting a radiopaquefluid such as, for example, Barium into the stomach and observing thefluid, for example, via x-ray imaging to determine proper flow betweenthe various regions of the stomach.

Once installation of the clamp is complete, the surgical equipment maybe removed, and the internal organs repositioned in their naturalpositions. Other precautions may be taken including, for example,cleaning or cauterizing any bleeding tissue to prevent clotting.

Magnetic Inserts

In some embodiments, the clamp may include insert portions to assistwith retaining the clamp in a substantially closed position. Forexample, FIGS. 56(a) and 56(b) illustrate an embodiment of a clamp 5600similar to the clamp 4100 described above, wherein the clamp 5600includes various insert portions 5601 for retaining the clamp 5600 in asubstantially closed position as illustrated in FIG. 56(a). The clamp5600, in one embodiment, includes first and second substrate members(not shown) and inserts 5601 (shown dashed) overmolded in a polymer orelastomer material to form a first elongated portion 5602, a secondelongated portion 5604, a bight portion 5606 (including a flexible hinge5618), a fastener portion 5608, and an engagement portion 5614.

The inserts 5601 may be used, in some embodiments, to engage the firstand second elongated portions 5602 and 5604 to partition a patient'sstomach in accordance with the present disclosure. For example, in someembodiments, the inserts 5601 may comprise magnets so that the insert5601 comprising the first elongated portion 5602 (shown in FIG. 56(a) as5601A) is capable of engaging the insert 5601 comprising the secondelongated portion 5602 (shown in FIG. 56(a) as 5601B) via a magneticforce to retain the clamp 5600 in a substantially closed position. Insome embodiments, both insert 5601A and insert 5601B are magnetic orcomprised of magnets having opposite polarities so that the inserts5601A are magnetically attracted to the inserts 5601B. In otherembodiments, one of insert 5601A or 5601B are magnetic, or comprised ofmagnets, and the other respective insert 5601A or 5601B is comprised ofa metallic material that is capable of being magnetically attracted tothe magnetic insert 5601 comprising the opposing elongated portion. Forexample, insert 5601A may comprise a magnet and insert 5601B maycomprise a metallic material that is capable of being magneticallyattracted to magnetic insert 5601A, and vice versa.

It should be appreciated that the inserts 5601 comprising one of theelongated portions of the clamp 5600 may be a single insert 5601 asillustrated in FIGS. 56(a) and 56(b). In other embodiments, the inserts5601 comprising one of the elongated portions may comprise a pluralityof inserts 5601 as illustrated in FIGS. 56(c) and 56(d). In yet anotherembodiment, a single insert 5601 may comprise one of the elongatedportions and a plurality of inserts 5601 may comprise the opposingelongated portion.

In some embodiments, the inserts 5601 may comprise a portion of thesubstrate member comprising one of the elongated portions of the clamp5600. For example, referring briefly to FIG. 57(a), the clamp 5600 isillustrated with a first substrate member 5701 comprising at least aportion of the first elongated portion 5602 and a second substratemember 5702 comprising at least a portion of the second elongatedportion 5604. In the embodiment illustrated in FIG. 57(a), the firstsubstrate member 5701 includes an insert 5601 disposed within a recess5703 formed in the first substrate member 5701. Similarly, the secondsubstrate member 5702 includes an insert 5601 disposed within a recess5703 formed in the second substrate member 5702. It should beappreciated that the embodiment illustrated in FIG. 57(a) may beimplemented with one insert 5601 in each of the respective substratemembers 5701 and 5702 as illustrated, or it may be implemented with aplurality of inserts 5601 in one or both of the respective substratemembers 5701 and 5702.

In some embodiments, the inserts 5601 may be positioned between asurface of the substrate member and the outside surface of theovermolding polymer or elastomer material. For example, referringbriefly to FIG. 57(b), the clamp 5600 is illustrated with a firstsubstrate member 5701 comprising at least a portion of the firstelongated portion 5602 and a second substrate member 5702 comprising atleast a portion of the second elongated portion 5604. In the embodimentillustrated in FIG. 57(b), the first elongated portion 5602 includes aninsert 5601 positioned between a surface 5704 of the first substratemember 5701 and the overmolding 5705. Similarly, the second elongatedportion 5604 includes an insert 5601 positioned between a surface 5706of the second substrate member 5702 and the overmolding 5705. It shouldbe appreciated that the embodiment illustrated in FIG. 57(b) may beimplemented with one insert 5601 in each of the respective elongatedportions 5602 and 5604 as illustrated, or it may be implemented with aplurality of inserts 5601 in one or both of the respective elongatedportions 5602 and 5604.

In yet another embodiment, the inserts 5601 may be embedded within asurface of the respective first and second elongated portions 5602 and5604. For example, referring briefly to FIG. 57(c), the clamp 5600 isillustrated with an insert 5601 embedded within a surface 5708 of thefirst elongated portion 5602, and an insert 5601 embedded within asurface 5710 of the second elongated portion 5604. It should beappreciated that the embodiment illustrated in FIG. 57(c) may beimplemented with one insert 5601 in each of the respective elongatedportions 5602 and 5604 as illustrated, or it may be implemented with aplurality of inserts 5601 in one or both of the respective elongatedportions 5602 and 5604.

The first and second elongated portions 5602 and 5604 serve as apartition-forming section located towards the distal end of thebariatric clamp 5600. Referring briefly to both FIGS. 56(a) and 10, whenthe clamp 5600 is installed within an abdominal cavity, the first andsecond elongated portions 5602 and 5604 are engaged via a magnetic forceto partition the patient's stomach into a small, vertical pouch 500 andan excluded section 502. The bight portion 5606 comprises apassage-forming section located towards the proximal end of the clamp5600. The passage-forming section allows gastric juices to flow 506 fromthe excluded section 502 into the vertical pouch 500.

Referring again to FIGS. 56(a)-56(d) and 57(a)-57(c), the first andsecond elongated portions 5602 and 5604 are joined by the bight portion5606, which is disposed generally at the proximal end of the clamp 5600.The bight portion 5606 includes a flexible hinge 5618 formed, in oneimplementation, from the polymer overmold. The flexible hinge 5618 isflexible and stretchable, thereby allowing the clamp 5600 to bepositioned in a variety of positions ranging from a substantially closedposition as illustrated in FIG. 56(a), to a substantially expanded (orfully opened) position. It should be appreciated that the flexible hinge5618 allows the clamp 5600 to flex, twist, contort, expand, stretch, orflex in virtually any desired angle or position.

When the clamp 5600 is installed, the flexible hinge 5618 permitsexpansion and movement of the bight portion 5606 to accommodate anyirregularities in the stomach wall or fluctuations of thepassage-forming section. The stretching or expanding of the flexiblehinge 5618 also allows the clamp 5600 to accommodate variations instomach thicknesses without compromising the pressure applied by theclamp 5600, particularly in the partition-forming section. In someembodiments, the flexible hinge 5618 may be provided at a desireddurometer or elasticity that may be the same as or different from thatof the polymer or silicone overmolded portions provided in other areasof the clamp 5600, such as the first and second elongated portions 5602and 5604.

The clamp 5600 may be installed in a manner consistent with thatdiscussed above with respect to the clamp 4100 and the methodsillustrated in FIGS. 45 and/or 47, except that the positioning of thefirst and second elongated portions 5602 and 5604 (as discussed withreference to block 4512 of FIG. 45) is performed such that a magneticattraction between the inserts 5601 engages the respective first andsecond elongated portions 5602 and 5604 to retain the clamp 5600 in asubstantially closed position to apply pressure to the stomach topartition a cavity inside the stomach. Similarly, the clamp 5600 may beuninstalled by reversing one or more of the steps for installing theclamp 5600, including disengaging the first and second elongatedportions 5602 and 5604 such that the magnetic force is broken betweenthe inserts 5601 comprising the respective first and second elongatedportions 5602 and 5604.

In some embodiments implementing inserts, the fastener portion andengagement portion may be eliminated. Examples of such embodiments areillustrated in FIGS. 58(a)-58(d), wherein the clamp 5800 is similar tothe clamp 5600 except that the clamp 5800 does not include the fastenerportion 5608 or the engagement portion 5614. The clamp 5800 doesinclude, however, first and second substrate members (not shown) andinserts 5801 (shown dashed) overmolded in a polymer or elastomermaterial to form a first elongated portion 5802, a second elongatedportion 5804, and a bight portion 5806 (including a flexible hinge5818).

The clamp 5800 may be installed in a manner consistent with thatdiscussed above with respect to the clamp 4100 and the methodsillustrated in FIGS. 45 and/or 47, except that the positioning of thefirst and second elongated portions 5802 and 5804 (as discussed withreference to block 4512 of FIG. 45) is performed such that a magneticattraction between the inserts 5801 engages the respective first andsecond elongated portions 5802 and 5804 to retain the clamp 5800 in asubstantially closed position to apply pressure to the stomach topartition a cavity inside the stomach. Similarly, the clamp 5800 may beuninstalled by reversing one or more of the steps for installing theclamp 5800, including disengaging the first and second elongatedportions 5802 and 5804 such that the magnetic force is broken betweenthe inserts 5801 comprising the respective first and second elongatedportions 5802 and 5804.

Curved Elongated Portions

In some embodiments, the clamp may include curved elongated members,wherein the curvature of the elongated members contours to the stomach'sexterior walls to provide better fit around the stomach. For example,FIGS. 59(a) and 59(b) illustrate an embodiment of a clamp 5900 similarto the clamp 4100 described above, wherein the clamp 5900 includescurved elongated members. The clamp 5900 includes first and secondsubstrate members (shown dashed in FIG. 59(b)) overmolded in a polymeror elastomer material to form a first elongated portion 5902, a secondelongated portion 5904, a bight portion 5906 (including a flexible hinge5918), a fastener portion 5908, and an engagement portion 5914.

As illustrated in FIG. 59(b), the curvature of the first elongatedportion 5902 and the second elongated portion 5904 is provided, at leastin part, by the curvature of the underlying substrate members.Specifically, the first substrate member 5910 forms the curvature of thefirst elongated portion 5902, and the second substrate member 5912 formsthe curvature of the second elongated portion 5904. In some embodiments,the curvature of the first and second elongated portions 5902 and 5904contours to the exterior walls of a patient's stomach to provide betterfit around the stomach.

The first and second elongated portions 5902 and 5904 serve as apartition-forming section located towards the distal end of thebariatric clamp 5900. Referring briefly to both FIGS. 59(a) and 10, whenthe clamp 5900 is installed within an abdominal cavity, the first andsecond elongated portions 5902 and 5904 are engaged to partition thepatient's stomach into a small, vertical pouch 500 and an excludedsection 502. The bight portion 5906 comprises a passage-forming sectionlocated towards the proximal end of the clamp 5900. The passage-formingsection allows gastric juices to flow 506 from the excluded section 502into the vertical pouch 500.

Referring again to FIGS. 59(a) and 59(b), the first and second elongatedportions 5902 and 5904 are joined by the bight portion 5906, which isdisposed generally at the proximal end of the clamp 5900. The bightportion 5906 includes a flexible hinge 5918 formed, in oneimplementation, from the polymer overmold. The flexible hinge 5918 isflexible and stretchable, thereby allowing the clamp 5900 to bepositioned in a variety of positions ranging from a substantially closedposition as illustrated in FIG. 59(a), to a substantially expanded (orfully opened) position. It should be appreciated that the flexible hinge5918 allows the clamp 5900 to flex, twist, contort, expand, stretch, orflex in virtually any desired angle or position.

Reference is now briefly made to FIGS. 60(a) and 60(b), wherein FIG.60(a) illustrates an example of a patient's stomach 6000, and FIG. 60(b)shows a cross section view of the stomach 6000 along the line A-Aprovided in FIG. 60(a). The stomach 6000 includes stomach walls 6010having an exterior surface 6012 and a generally curved shape.

When the clamp 5900 is installed, as shown in FIG. 61, the curvature ofthe first and second elongated portions 5902 and 5904 contours to thewalls 6010 and exterior surface 6012 of the stomach 6000. The curvatureof the first and second elongated portions 5902 and 5904 allows for abetter fit around the stomach 6000 while still forming a partition 6102within the stomach 6000. As discussed above, the bight portion 5906forms a passage 6104 in the stomach 6000 to allow gastric juices to flowbetween the excluded section of the stomach 6000 and the vertical pouchof the stomach 6000.

As shown in FIG. 61, the flexible hinge 5918 permits expansion andmovement of the bight portion 5906 to accommodate any irregularities inthe stomach wall 6010 or fluctuations of the passage 6104. Thestretching or expanding of the flexible hinge 5918 also allows the clamp5900 to accommodate variations in stomach thicknesses withoutcompromising the pressure applied by the clamp 5900, particularly in thepartition-forming section. In some embodiments, the flexible hinge 5918may be provided at a desired durometer or elasticity that may be thesame as or different from that of the polymer or silicone overmoldedportions provided in other areas of the clamp 5900, such as the firstand second elongated portions 5902 and 5904.

It should be appreciated that clamp 5900 may be installed anduninstalled in a manner consistent with that discussed above withrespect to the clamp 4100 and the methods illustrated in FIGS. 45 and47. When positioning the first and second elongated portions 5902 and5904, however, the elongated portions may be positioned such that thecurvature of the respective first and second elongated portions 5902 and5904 are aligned to conform to the curvature of the stomach walls 6010.

Cross-Sectional Views

Reference is now made to FIGS. 62 and 63(a)-63(n), which are used incombination to illustrate that any of the clamp embodiments disclosedherein may have any cross-sectional shape, including those explicitlyillustrated in FIGS. 63(a)-63(n). FIG. 62 illustrates an exemplaryembodiment of a clamp 6200 representative of any of the embodimentsdiscussed herein. The clamp 6200 includes a first elongated portion 6210and a second elongated portion 6220. FIGS. 63(a)-63(n) illustratevarious examples of representative cross-sectional views of the firstelongated portion 6210 of clamp 6200 as viewed along line A-A of FIG.62. It should be appreciated that the example cross-sectional viewsillustrated in FIGS. 63(a)-63(n) may be representative of thecross-sectional shape of the polymer overmolding, the substrate member,or both. It should also be appreciated that the example cross-sectionalviews illustrated in FIGS. 63(a)-63(h) may be representative of thecross-sectional shape of any other portions of the clamp 6200 including,for example, the second elongated portion 6220.

FIG. 63(a) illustrates an example cross-sectional view having a rounded,or circular, shape 6301. FIG. 63(b) illustrates an examplecross-sectional view having a rectangular shape 6302. FIG. 63(c)illustrates an example cross-sectional view having a plano-convex shape6303, wherein the shape has a convex surface 6303(a), a planar surface6303(b), and side portions 6303(c). FIG. 63(d) illustrates an examplecross-sectional view having a biconvex shape 6304, wherein the shape hasa first convex surface 6304(a), a second convex surface 6304(b), andside portions 6304(c). FIG. 63(e) illustrates an example cross-sectionalview having a biconcave shape 6305, wherein the shape has a firstconcave surface 6305(a), a second concave surface 6305(b), and sideportions 6305(c). FIG. 63(f) illustrates an example cross-sectional viewhaving a plano-concave shape 6306, wherein the shape has a planarsurface 6306(a), a concave surface 6306(b), and side portions 6306(c).FIG. 63(g) illustrates an example cross-sectional view having a positivemeniscus shape 6307, wherein the shape has a convex surface 6307(a), aconcave surface 6307(b) having a radius of curvature that is larger thanthat of the convex surface 6307(a), and side portions 6307(c). FIG.63(h) illustrates an example cross-sectional view having a negativemeniscus shape 6308, wherein the shape has a convex surface 6307(a), aconcave surface 6308(b) having a radius of curvature that is less thanthat of the convex surface 6308(a), and side portions 6308(c). FIG.63(i) illustrates an example cross-sectional view having an elongatedrounded, or oval, shape 6309 oriented with its length in a verticalposition. FIG. 63(j) illustrates an example cross-sectional view havingan elongated rounded, or oval, shape 6310 oriented with its length in ahorizontal position. FIG. 63(k) illustrates an example cross-sectionalview having an octagonal shape 6311. FIG. 63(l) illustrates an examplecross-sectional view having a hexagonal shape 6312. FIG. 63(m)illustrates an example cross-sectional view having a triangular shape6313. FIG. 63(n) illustrates an example cross-sectional view having aplano-convex shape 6314, wherein the shape has a planar surface 6314(a),a convex surface 6314(b), and no side portions.

It should be appreciated that the cross-sectional shape of the clamp isnot limited to those illustrated in FIGS. 63(a)-63(n) and discussedabove. For example, the cross-sectional shape can be any shape and evenany combination of shapes, including combinations those shapes discussedabove with respect to FIGS. 63(a)-63(n). Furthermore, thecross-sectional shapes discussed above and illustrated in FIGS.63(a)-63(n) may be oriented in any direction or orientation, and are notlimited to those shown in FIGS. 63(a)-63 (n).

Suture Portions

FIG. 64 illustrates an example embodiment of a polymer overmoldedbariatric clamp 6400 having suture portions 6402 formed therein. Theclamp 6400 is similar to that discussed above with respect to the clamp4100 of FIG. 41, except that the clamp 6400 includes suture portions6401. The clamp 6400 includes first and second substrate members (notshown) overmolded in a polymer or elastomer material to form a firstelongated portion 6402, a second elongated portion 6404, a bight portion6406 (including a flexible hinge 6418), a fastener portion 6408, and anengagement portion 6414. As discussed below, the suture portions 6401are formed, in some embodiments, by the polymer overmold overlayingrecesses formed in the substrate members comprising the first and secondelongated portions 6402 and 6404, thereby forming polymer regions thatare capable of being penetrated by a suture needle to affix the clamp6400 to the stomach. In other embodiments, the polymer may not encompassthe recesses such that the recesses remain unobstructed to provide anopening in the underlying substrate member to receive sutures foraffixing the clamp 6400 to the stomach and/or other tissue. In otherwords, the suture portion 6401 may comprise a recess or opening throughboth the polymer overmolding and the underlying substrate member.

FIG. 65 illustrates the clamp 6400, wherein the polymer overmolding isillustrated semitransparent to show the first substrate member 6502comprising at least a portion of the first elongated portion 6402 and aportion of the bight portion 6408, and the second substrate member 6504comprising at least a portion of the second elongated portion 6404 and aportion of the bight portion 6408.

FIGS. 66(a) and 66(b) illustrate example embodiments of the respectivefirst substrate member 6502 and second substrate member 6504. Thesubstrate members 6502 and 6504 are shown from a profile view in FIG.66(a), and are shown from a top view in FIG. 66(b). The substratemembers 6502 and 6504 are similar to those discussed above with respectto FIGS. 31(a) and 31(b) except that the substrate members 6502 and 6504have been modified to include recesses 6602 formed in the substratemembers 6502 and 6504.

The recesses 6602 are openings through the respective substrate member6502 or 6504 that are capable of receiving a suture, staple, or otherapparatus to affix the clamp 6400 to the stomach and/or other tissue.This may include affixing the clamp 6400 to itself alone or incombination with affixing the clamp 6400 to the stomach and/or othertissue. In some embodiments, the recesses 6602 may also include openingsin the overmolding such that the suture portion 6401 is a recess throughboth the polymer overmolding and the underlying substrate member6502/6504. The recesses 6602 may be formed at different locations of thesubstrate members 6502/6504 including, for example, along sides of theelongated portions 6402/6404, along sides of the bight portion 6408, atends of the substrate members 6502/6504 near the proximal end of theclamp 6400, and at ends of the substrate members 6502/6504 near thedistal end of the clamp 6400. FIG. 66(b) shows recesses 6602(a) disposedat ends of the substrate members 6502 and 6504 near the proximal end ofthe clamp 6400, and recesses 6602(b) disposed at ends of the substratemembers 6502 and 6504 near the distal end of the clamp 6400.

In some embodiments, the recesses 6602 are formed in the substratemember 6502 or 6504 such that the perimeter of a recess 6602 is definedby the substrate member 6502 or 6504. For example, FIGS. 67(a)-67(c)show various views of an embodiment of the clamp 6400 with a portion ofthe overmolding removed to show a portion of the underlying substrate6504. As shown in FIGS. 67(a)-67(c), the recess 6602 has a perimeterdefined, at least partially, by the underlying substrate 6504.Furthermore, the underlying substrate member 6504 includes a portion6504(a) that is capable of retaining a suture in the recess 6602 toprevent the clamp 6400 from disconnecting from the tissue to which it issutured. Without the retaining portion 6504(a), a suture could tearthrough the overmolding, causing the clamp 6400 to become disconnected.

FIG. 68 illustrates an example view of the first elongated portion 6402and bight portion 6408 of the clamp 6400 having suture portions 6401.

FIG. 69 illustrates an example view of the second elongated portion 6404and bight portion 6408 of the clamp 6400 having suture portions 6401,wherein a portion of the overmolding is partially removed to show theunderlying substrate member 6504.

As discussed above, the first and second elongated portions 6402 and6404 serve as a partition-forming section of the bariatric clamp 6400.Referring briefly to both FIGS. 64 and 10, when the clamp 6400 isinstalled within an abdominal cavity, the first and second elongatedportions 6402 and 6404 are engaged to partition the stomach into asmall, vertical pouch 500 and an excluded section 502. The bight portion6406 comprises a passage-forming section located towards the proximalend of the clamp 6400. The passage-forming section allows gastric juicesto flow 506 from the excluded section 502 into the vertical pouch 500.

As shown in FIG. 64, the first and second elongated portions 6402 and6404 are joined by the bight portion 6406, which is disposed generallyat the proximal end of the clamp 6400. The bight portion 6406 includes aflexible hinge 6418 formed, in one implementation, from the polymerovermold. The flexible hinge 6418 allows the clamp 6400 to be positionedin a variety of positions ranging from a substantially closed positionto a substantially expanded (or fully opened) position. It should beappreciated that the flexible hinge 6418 allows the clamp 6400 to flex,twist, contort, expand, stretch, or flex in virtually any desired angleor position.

When the clamp 6400 is installed, the flexible hinge 6418 permitsexpansion and movement of the bight portion 6406 to accommodate anyirregularities in the stomach wall or fluctuations of thepassage-forming section. The stretching or expanding of the flexiblehinge 6418 also allows the clamp 6400 to accommodate variations instomach thicknesses without compromising the pressure applied by theclamp 6400, particularly in the partition-forming section. In someembodiments, the flexible hinge 6418 may be provided at a desireddurometer or elasticity that may be the same as or different from thatof the polymer or silicone overmolded portions provided in other areasof the clamp 6400, such as the first and second elongated portions 6402and 6404.

The clamp 6400 may be installed in a manner consistent with thatdiscussed above with respect to the clamp 4100 and the methodsillustrated in FIGS. 45 and/or 47. Similarly, the clamp 6400 may beuninstalled by reversing one or more of the steps for installing theclamp 6400.

Bight Portion

It should be appreciated that, in some embodiments, the disclosed clampmay have an opening (occasionally referred to herein as “slottedaperture”) in the bight portion or flexible hinge. For example, FIG. 70illustrates an example embodiment of a clamp 7000 in accordance with anyembodiment disclosed herein, wherein the clamp 7000 includes an opening7002 in the flexible hinge 7004 of the bight portion 7006. Someembodiments may not include such an opening. In some instances, when theclamp 7000 is installed, a suture may be applied at the opening 7002 toaffix the bight portion 7006 of the clamp 7000 to the stomach. If thestomach or clamp 7000 moves or adjusts, the suture may tear through theflexible hinge 7004, which is typically comprised of the overmolding,thereby causing the clamp 7000 to partially disconnect or becomeuninstalled from the patient's stomach.

Embodiments of the disclosed clamp 7000 may include certain features toprevent the suture installed at the opening 7002 from tearing the clamp7000. For example, in some embodiments, the flexible hinge may includeone or more substrate members embedded within the overmolding formingthe flexible hinge 7004. Such examples are illustrated in FIGS. 71-73,which illustrate views of the opening 7002 in the flexible hinge 7004 ofthe clamp 7000 in FIG. 70. In some embodiments, the one or moresubstrate members are comprised of a substance capable of withstandingthe cutting force of a suture installed at the opening 7002 or theflexible hinge 7004. Examples of such a substance include metal,plastic, rubber, or even a portion of the overmolding having a durometergreat enough to withstand the cutting force of the suture.

In FIG. 71, the flexible hinge 7004 includes embedded substrate members7101-7104 (shown dashed) each comprised of a substance capable ofwithstanding the cutting force of a suture installed at the opening 7002or otherwise at the flexible hinge 7004. In the event a suture cuts ortears through the overmolding comprising the flexible hinge 7004, one ormore of the embedded substrate members 7101-7104 are capable ofretaining the suture within the area defined by the substrate members7101-7104, thereby preventing further damage to the clamp 7000 andretaining the clamp 7000 as installed on the patient's stomach.

As shown in FIG. 71, the substrate members 7101-7104 are positioned in arectangular orientation around the opening 7002. Because the flexiblehinge 7004 is capable of flexing, twisting, stretching, and otherwisecontorting, the substrate members 7101-7104 are not attached to eachother to allow for the flexible hinge 7004 to contort or stretch invarious directions without substantially impeding such movement of theflexible hinge 7004. In some embodiments, the substrate members7101-7104 may be integrated. In such embodiments, the substrate members7101-7104 may be comprised of a material that is capable of stretchingor contorting and is also capable of withstanding the cutting force of asuture installed in the opening 7002 or otherwise at the flexible hinge7004.

In FIG. 72, the flexible hinge 7004 includes embedded substrate members7201 and 7202 (shown dashed) each comprised of a substance capable ofwithstanding the cutting force of a suture installed at the opening 7002or otherwise at the flexible hinge 7004. In the event a suture cuts ortears through the overmolding comprising the flexible hinge 7004, one ormore of the embedded substrate members 7201 and 7202 are capable ofretaining the suture within the area defined by the substrate members7201 and 7202, thereby preventing further damage to the clamp 7000 andretaining the clamp 7000 as installed on the patient's stomach.

As shown in FIG. 72, the substrate members 7201 and 7202 each have ahorseshoe or U-shaped configuration positioned to overlap around theopening 7002. Because the flexible hinge 7004 is capable of flexing,twisting, stretching, and otherwise contorting, the substrate members7201 and 7202 are not attached to each other to allow for the flexiblehinge 7004 to contort or stretch in various directions withoutsubstantially impeding such movement of the flexible hinge 7004.Furthermore, the substrate members 7201 and 7202 overlap each other suchthat, if the flexible hinge 7004 is stretched as shown in FIG. 73, thesubstrate members 7201 and 7202 still encompass the perimeter of theopening 7002. In some embodiments, the substrate members 7201 and 7202may be integrated. In such embodiments, the substrate members 7201 and7202 may be comprised of a material that is capable of stretching orcontorting and is also capable of withstanding the cutting force of asuture installed in the opening 7002 or otherwise at the flexible hinge7004.

FIG. 74 illustrates an example embodiment of the clamp 7000, wherein theflexible hinge 7004 includes a wired member 7400 at least partiallyembedded within the overmolding. As shown in FIG. 74, the clamp 7000includes a first substrate member 7402 and a second substrate member7404 (both shown dashed) in accordance with an example embodiment of thepresent disclosure. The wired member 7400 is coupled at a first end 7401to the first substrate member 7402, and is coupled at a second end 7403to the second substrate member 7404. For example, the first substratemember 7402 may have an opening or recess 7406 located toward an end ofthe first substrate member 7402 through which the first end 7401 of thewired member 7400 may be inserted. Similarly, the second substratemember 7404 may have an opening or recess 7408 located toward an end ofthe second substrate member 7404 through which the second end 7403 ofthe wired member 7400 may be inserted. It should be appreciated that thewired member may be coupled to the first and second substrate members7402 and 7404 (or to other components) in various other ways other thanthose disclosed herein.

As shown in FIG. 74, the wired member 7400 further includes a ringportion 7405 inserted proximate the opening 7002. In some embodiments,the ring portion 7405 is embedded within the overmolding and ispositioned around the circumference of the opening 7002. FIG. 75illustrates such an embodiment wherein the clamp 7000 is shown from anend view wherein the ring portion 7405 is embedded within theovermolding forming the flexible hinge 7004 and positioned around thecircumference, or perimeter, of the opening 7002. In other embodiments,the ring portion 7405 may be positioned outside of the overmolding andwithin the perimeter of the opening 7002. FIG. 76 illustrates such anembodiment wherein the clamp 7000 is shown from an end view wherein thering portion 7405 is positioned outside of the overmolding and withinthe perimeter of the opening 7002.

The wired member 7400, and specifically the ring portion 7405, iscomprised of a substance (e.g., metal wiring) capable of withstandingthe cutting force of a suture installed at the opening 7002 or theflexible hinge 7004. In the event a suture cuts or tears through theovermolding comprising the flexible hinge 7004, the wire member 7400 iscapable of retaining the suture within the area defined by the ringportion 7405 (or preventing the suture from tearing through the flexiblehinge 7004), thereby preventing further damage to the clamp 7000 andretaining the clamp 7000 as installed on the patient's stomach. Itshould also be appreciated that the wired member 7400 is capable ofreinforcing the strength and durability of the flexible hinge 7004 andopening 7002 while still allowing for flexibility of the hinge 7004.

In some embodiments, the wired member 7400 may include extra slack inthe wire to allow the flexible hinge 7004 to stretch. An example of suchan embodiment is illustrated in FIGS. 77 and 78. In FIG. 77, theflexible hinge 7004 is shown in a relaxed position, wherein the wiredmember 7400 includes extra slack 7700 embedded within the flexible hinge7004. In FIG. 78, the flexible hinge 7004 is shown in a stretchedposition, wherein the extra slack 7700 of the wired member 7400 isutilized to allow the flexible hinge 7004 to stretch.

In some embodiments, the opening 7002 of the clamp 7000 may include aneyelet disposed within the area of the opening 7002. An example of suchan embodiment is illustrated in FIG. 79, wherein the clamp 7000 includesan eyelet 7900 disposed within the area of the opening 7002 in theflexible hinge 7004. In some embodiments, the eyelet 7900 may includearms 7902 that extend into the overmolding of the flexible hinge 7004 toposition the eyelet 7900 within the opening 7002 and to anchor theeyelet 7900 into the flexible hinge 7004. In some embodiments, theeyelet 7900 may further include protrusions 7904 coupled to the arms7902 and protruding into the flexible hinge 7004 to further anchor theeyelet 7900 into the flexible hinge 7004.

The eyelet 7900 includes an opening 7905 for receiving a suture, and maybe comprised of a substance capable of withstanding the cutting force ofa suture installed within the opening 7905 of the eyelet 7900. Theeyelet 7900 prevents the suture from tearing through the opening 7002 orthe flexible hinge 7004. Furthermore, the eyelet 7900 is disposed withinthe area of the opening 7002 and, therefore, does not prevent theopening 7002 or flexible hinge 7004 from stretching, twisting, flexing,or otherwise contorting.

In some embodiments, the clamp 7000 may include a separate portion orplate that is capable of being applied over the bight portion 7006 orflexible hinge 7004 of the clamp 7000 and then sutured to the clamp 7000and stomach (or to the stomach only) to provide reinforcement to theflexible hinge 7004 and/or bight portion 7006 of the clamp 7000. Theseparate plate may be of various sizes depending upon the size of thepatient's stomach, and may be comprised of titanium or other materialcapable of withstanding the cutting force of a suture. Such an exampleis illustrated in FIGS. 80(a) and 80(b), wherein a plate 8000 is shownseparate from the clamp 7000 in FIG. 80(a), and is shown installed overthe bight portion 7006 of the clamp 7000 in FIG. 80(b). The plate 8000may include one or more recesses 8001 for coupling the plate 8000 to thestomach or to the bight portion 7006 of the clamp 7000.

In some embodiments, the bight portion may include a T-fastener (ortoggle suture) at least partially embedded within the flexible hinge andhaving a ring portion through which a suture may be applied to affix theclamp to the stomach during installation and/or to secure the clamp inplace after it is installed. FIG. 81 illustrates an example embodimentof a clamp 8100 having a T-fastener 8102 embedded at least partiallywithin the flexible hinge 8104 of the clamp 8100. Coupled to theT-fastener 8102 is a ring portion 8106 through which a suture may bepassed to affix the clamp 8100 to a patient's stomach. In such anembodiment, the flexible hinge may or may not include an opening.Similarly, FIG. 82 illustrates an embodiment of a clamp 8200 having aring portion 8206 looping through suture portions of the flexible hinge8204 of the clamp 8200. So as to facilitate easy installation of theclamp 8200, a suture may be passed through the ring portion 8206 toaffix the clamp 8200 to the patient's stomach. An example of such asuture technique is discussed in U.S. Pat. No. 6,596,014, which ishereby incorporated by reference for all purposes.

In some embodiments, a suture string may be pre-attached to the clampfor use in affixing the clamp the patient's stomach. FIG. 83 illustratesan embodiment of a clamp 8300 having barbed suture strings 8306 affixedto suture portions. The barbed suture strings 8306 have hooks at adistal end thereof to facilitate suturing to the patient's stomach. Thebarbs of the suture strings 8306 help prevent the suture strings 8306from being pulled out, for example during expansion of the stomachcaused by the patient consuming an amount of food that causes stretchingof the stomach. In other embodiments, for example as shown in FIG. 84,the suture strings 8406 may not be barbed, and also may have T-fastenersas described above affixed to the distal ends thereof. The T-fastenersare passed through the patient's stomach during suturing of the clamp8400 to the patient's stomach, and act to prevent the suture strings8306 from being pulled out.

Inflatable Portions

In some embodiments, the clamp may include inflatable portions to assistwith positioning or retaining the clamp on a patient's stomach when theclamp is installed in a substantially closed position. For example,FIGS. 85(a) and 85(b) illustrate an embodiment of a clamp 8500 similarto the clamp 4100 described above, wherein the clamp 8500 includesvarious inflatable portions 8501 (shown as dashed portions 8501A and8501B) for positioning or retaining the clamp 8500 in a substantiallyclosed position. The clamp 8500, in one embodiment, includes first andsecond substrate members (not shown) overmolded in a polymer orelastomer material to form a first elongated portion 8502, a secondelongated portion 8504, a bight portion 8506 (including a flexible hinge8518), a fastener portion 8508, and an engagement portion 8514. Theinflatable portions 8501 are shown in a deflated state in FIGS. 85(a)and 85(b), and are shown dashed to indicate that they are positioned inthe polymer overmolding. Although, in some embodiments, the inflatableportions may be positioned outside of the polymer overmolding.

The clamp 8500 and portions of the clamp 8500, and other similar clampsand similar portions of those clamps, may be used as discussed herein inaccordance with the foregoing disclosure (e.g., to partition thestomach, to allow flexing with the flexible hinge 8518, to be installedvia trocar, to be installed in an expanded/open position, to retain theclamp 8500 in a closed position, etc.), but with the added benefitsprovided by the inflatable portions 8501. For example, the first andsecond elongated portions 8502 and 8504 generally form apartition-forming section of the clamp 8500, and the bight portion 8506generally forms a passage-forming section of the clamp 8500, as shouldbe understood from the foregoing disclosure. The partition-forming andpassage-forming sections (and the clamp 8500, in general) operate inaccordance with the disclosure provided for other clamp embodimentsdiscussed herein. In embodiments of the clamp featuring the inflatableportions 8501, however, the pressure applied by the partition-formingsection of the clamp 8500 may be provided by the air pressure inside theinflatable portions 8501. In some embodiments, this air pressure may beadjusted to provide a customized or modified application or fit of theclamp on the patient's stomach.

Although it is not illustrated in FIG. 85(a) or 85(b), it should beunderstood that, in some embodiments, the inflatable portions 8501 maybe inflated and deflated using a port connected to one or more of theinflatable portions 8501 via a tube as shown in FIGS. 86-89. The port(s)may be located proximate the clamp 8500 as shown in FIGS. 86-88, or, asshown in FIG. 89, the port(s) may be a subcutaneous port that isaccessible from outside the patient's body and extended from the clamp8500 via one or more tubes coupled to the inflatable portions 8501. Theport(s) and tube(s) discussed herein are provided to facilitateinflation and/or deflation of the inflatable portions 8501. Air may beintroduced or expelled at the port(s). Introduced air travels into theport(s) and along the tube(s) to inflate the inflatable portions 8501.Air that is expelled travels from the inflatable portions 8501 along thetube(s) and out the port(s).

In some embodiments, the inflatable portions 8501 are disposed alonginterior sections 8515 of the first and second elongated portions 8502and 8504, generally along the partition-forming section of the clamp8500. For example, FIGS. 85(a), 85(b), 86, and 87 illustrate embodimentswhere one or more of the inflatable portions 8501A and 8501B arepositioned or embedded within the polymer overmolding of the respectivefirst and second elongated portions 8502 and 8504. In such embodiments,the polymer overmolding may include one or more slits or openings (notshown) to allow the inflatable portion 8501 to protrude from the polymerovermolding when the inflatable portion 8501 is inflated to provide acushion between the clamp 8500 and the stomach of a patient. In otherembodiments, one or more of the inflatable portions may be positionedoutside the polymer overmolding in both inflated and deflated states. Insuch embodiments, the ports and/or tubes may be positioned eitheroutside the polymer overmolding, or within the polymer overmolding asdiscussed herein.

In FIG. 86, the inserts 8501 are shown positioned within a portion ofthe substrate member comprising one of the elongated portions of theclamp 8500. For example, the clamp 8500 is illustrated with a firstsubstrate member 8601 comprising at least a portion of the firstelongated portion 8502 and a second substrate member 8602 comprising atleast a portion of the second elongated portion 8504. In the embodimentillustrated in FIG. 86, the first substrate member 8601 includesinflatable portion 8501A disposed within a recess 8603 formed in thefirst substrate member 8601. Similarly, the second substrate member 8602includes inflatable portion 8501B disposed within a recess 8604 formedin the second substrate member 8602. It should be appreciated that theembodiment illustrated in FIG. 86 may be implemented with one inflatableportion 8501 in each of the respective substrate members 8601 and 8602as illustrated, or it may be implemented with a plurality of inflatableportions 8501 in one or both of the respective substrate members 8601and 8602.

As shown in FIG. 86, the first inflatable portion 8501A is inflatedand/or deflated using a port 8610A positioned on the first elongatedportion 8502. The port 8610A is positioned on a surface (e.g., anexternal surface 8615) of the first elongated portion 8502 and iscoupled to the first inflatable portion 8501A via a tube 8612A embeddedin the polymer overmolding (thereby forming a chamber 8611A within thepolymer overmolding, the chamber 8611A containing the tube 8612A) andconnected to the first inflatable portion 8501A at an interface 8613A.Similarly, the second inflatable portion 8501B is inflated and/ordeflated using a port 8610B positioned on the second elongated portion8504. The port 8610B is positioned on a surface (e.g., an externalsurface 8615) of the second elongated portion 8504 and is coupled to thesecond inflatable portion 8501B via a tube 8612B embedded in the polymerovermolding (thereby forming a chamber 8611B within the polymerovermolding, the chamber 8611B containing the tube 8612B) and connectedto the second inflatable portion 8501B at an interface 8613B. In someembodiments, the clamp 8500 may have a single port 8610 coupled to allof the inflatable portions 8501 via a plurality of tubes 8612. Anexample of one such embodiment is provided in FIG. 87. It should beappreciated, however, that all clamp embodiments having inflatableportions may include an implementation having one or multiple ports(including subcutaneous ports) and tubes, and that the port(s) may bepositioned in any location on the clamp 8500 that does not interferewith operation or installation of the clamp 8500.

The ports 8610 and tubes 8612 are provided to facilitate inflation anddeflation of the inflatable portions 8501. Air may be introduced orexpelled at the ports 8610. Introduced air travels into the ports 8610and along the tubes 8612 to inflate the inflatable portions 8501. Airthat is expelled travels from the inflatable portions 8501 along thetubes 8612 and out the ports 8610. In some embodiments, the tubes 8612may be positioned along or within respective ones of the substratemembers 8601 and 8602 to provide alignment and/or protection of therespective tubes 8612. For example, a tube 8612 positioned within asubstrate member 8601/8602 may be protected from external pressures orforces by the structure of the substrate member 8601/8602.

FIG. 87 illustrates another embodiment of the clamp 8500, wherein one ormore of the inflatable portions 8501A and 8501B are positioned orembedded within the polymer overmolding of the respective first andsecond elongated portions 8502 and 8504. As shown in FIG. 87, theinflatable portions 8501 may be positioned between a surface of thesubstrate member and the interior surface of the overmolding polymer orelastomer material. For example, the clamp 8500 is illustrated in FIG.87 with a first substrate member 8601 comprising at least a portion ofthe first elongated portion 8502 and a second substrate member 8602comprising at least a portion of the second elongated portion 8504. Inthe embodiment illustrated in FIG. 87, the first elongated portion 8502includes an inflatable portion 8501A positioned between a surface 8704of the first substrate member 8601 and the interior surface 8705 of theovermolding. Similarly, the second elongated portion 8604 includes aninflatable portion 8501B positioned between a surface 8706 of the secondsubstrate member 8602 and the interior surface 8705 of the overmolding.

Similar to the clamp embodiment shown in FIG. 86, the first and secondinflatable portions 8501 are inflated and/or deflated using a port 8610and one or more tubes 8612. In the embodiment illustrated in FIG. 87,however, there is a single port 8610 shared by both inflatable portions8501. The port 8610 is positioned on the bight portion 8506 and coupledto the first and second inflatable portions 8501 via tubes 8612 in thepolymer overmolding. The clamp 8500 includes one or more chambers 8611defined within the polymer overmolding, wherein the chambers 8611contain the tubes 8612. In FIG. 87, a first tube 8612A extends from theport 8610 along a first chamber 8611A in the bight portion 8506 andfirst elongated portion 8502 and is connected to the first inflatableportion 8501A at an interface 8613A. Similarly, a second tube 8612Bextends from the port 8610 along a second chamber 8611B in the bightportion 8506 and second elongated portion 8504 and is connected to thesecond inflatable portion 8501B at an interface 8613B.

FIG. 88 illustrates another embodiment of the clamp 8500, wherein one ormore of the inflatable portions 8501 are positioned along the interiorsections 8515 at interior surfaces 8815 of the polymer overmolding ofthe respective first and second elongated portions 8502 and 8504. Asshown in FIG. 88, the first inflatable portion 8501A is positioned onthe interior surface 8815A of the first elongated portion 8502.Similarly, the second inflatable portion 8501B is positioned on theinterior surface 8815B of the second elongated portion 8504. Similar tothe embodiment shown in FIG. 86, the first inflatable portion 8501A isinflated and/or deflated using a port 8610A positioned on the firstelongated portion 8502. The port 8610A is positioned on an externalsurface 8817 of the first elongated portion 8502 and is coupled to thefirst inflatable portion 8501A via a tube 8612A positioned within achamber 8611A in the polymer overmolding (in some embodiments, thechamber 8611A may also extend through a substrate member). The tube8612A is connected to the first inflatable portion 8501A at an interface8613A. Similarly, the second inflatable portion 8501B is inflated and/ordeflated using a port 8610B positioned on the second elongated portion8504. The port 8610B is positioned on an external surface 8819 of thesecond elongated portion 8504 and is coupled to the second inflatableportion 8501B via a tube 8612B positioned within a chamber 8611B in thepolymer overmolding (in some embodiments, the chamber 8611B may alsoextend through a substrate member). The tube 8612B is connected to thesecond inflatable portion 8501B at an interface 8613B.

Referring briefly to FIG. 89, an example embodiment of the clamp 8500 isshown installed on a patient's stomach 8902 and implemented with asubcutaneous port 8910. The subcutaneous port 8910 is accessible fromoutside the patient's body 8900 and is extended from the clamp 8500 viaone or more tubes 8612 coupled to the inflatable portions 8501 asdiscussed in accordance with any of the disclosed embodiments providedherein. The port 8910 and tube 8612 are provided to facilitate inflationand/or deflation of the inflatable portions 8501 of the clamp 8500. Airmay be introduced or expelled at the port 8910. Introduced air travelsinto the port 8910 and along the tube 8612 to inflate the inflatableportions 8501. Air that is expelled travels from the inflatable portions8501 along the tube 8612 and out the port 8910. It should be appreciatedthat the subcutaneous port may be implemented with any of theembodiments disclosed herein. In some embodiments, the subcutaneous port8910 and tube 8612 may be used to adjust the pressure in the inflatableportions 8501 of the clamp 8500.

Referring now to FIG. 90, a representative embodiment of the clamp 8500is shown with the inflatable portions 8501 in an inflated state. Wheninflated, the inflatable portions 8501 may be used, in some embodiments,to cushion the clamp 8500 against the stomach of a patient once theclamp has been installed in a closed position on the stomach. Thiscushion allows for the clamp 8500 to be secured in place on the stomachand to accommodate irregularities in the stomach wall while also forminga partition within the stomach. In some embodiments, the air pressure inthe inflatable portions 8501 may be adjusted as desired to provide acustomized fit on the stomach and to adjust the pressure applied to thestomach by the partition-forming section of the clamp 8500. It should beunderstood that the advantages and benefits discussed herein withrespect to the inflatable portions is applicable to all clampembodiments incorporating the inflatable portions, and not just thoseassociated with the specifically described reference numerals.

It should be appreciated that the inflatable portions may beincorporated in any of the disclosed clamp embodiments provided herein.For example, FIG. 91 illustrates an example embodiment of a clamp 9100similar to the clamp 7000 discussed above with respect to FIG. 70. Theclamp 9100 includes inflatable portions 9101 (shown in an inflatedstate), wherein a first inflatable portion 9101A is positioned along afirst elongated portion 9102 of the clamp 9100, and a second inflatableportion 9101B is positioned along a second elongated portion 9104 of theclamp 9100. The example embodiment of the clamp 9100 illustrated in FIG.91 features a port 9110 positioned at the bight portion 9106 of theclamp 9100. In accordance with the foregoing disclosure, the port 9110is provided to facilitate inflation and/or deflation of the inflatableportions 9101 via tubes (not shown). Air may be introduced or expelledat the port 9110. Introduced air travels into the port 9110 and alongthe tubes (not shown) to inflate the inflatable portions 9101. Air thatis expelled travels from the inflatable portions 9101 along the tubesand out the port 9110. It should be appreciated that the clamp 9100 maybe implemented, in alternate embodiments, with ports 9110 positioned onthe first and second elongated portions 9102 and 9104, or having asubcutaneous port.

Inflatable Substrate Members

In some embodiments, the inflatable portions may provide a substitutefor all, or portions of, the rigid substrate members included in any ofthe clamp embodiments provided herein. In such embodiments where theinflatable portions are used as a substitute for rigid substratemembers, the clamp may be considered as having inflatable substratemembers. These inflatable substrate members function in substantiallythe same manner as the rigid substrate members, except the inflatablesubstrate members are more flexible, provide the advantages discussedabove with respect to inflatable portions, may be adjusted in someembodiments to provide varying levels of inflation/pressure, and may beinstalled in a deflated form that permits the clamp to be more flexibleto facilitate an easier installation. For example, FIG. 92 illustratesan embodiment of a clamp 9200 similar to the clamp 4100 described above,wherein the clamp 9200 includes inflatable portions 9202A and 9202B(shown dashed) as substitutes for the rigid substrate members 4101 and4103 in FIG. 41(a). The clamp 9200 operates similar to the clamp 4100,except that the rigid substrate members 4101 and 4103 are replaced withinflatable portions 9202A and 9202B.

The clamp 9200, in one embodiment, comprises a polymer material andincludes a first elongated portion 9214, a second elongated portion9216, a bight portion 9218 (including a flexible hinge 9220 formed bythe polymer material), a fastener portion 9222, and an engagementportion 9224. The clamp 9200 also includes a first inflatable portion9202A that is inflated and/or deflated using a port 9204A coupled to thefirst inflatable portion 9202A via a tube 9206A. The tube 9206A andinflatable portion 9202A are positioned within a chamber 9210A formed inthe polymer material and are coupled together at an interface 9208A. Inits inflated state, the first inflatable portion 9202A generally fillsthe chamber 9210A and takes the shape of the rigid substrate member 4101(see FIG. 41(a)) and functions in a manner similar to the substratemember 4101 as discussed above. When deflated, the first inflatableportion 9202A is positioned within the chamber 9210A in a flaccid state.

The clamp 9200 also includes a second inflatable portion 9202B that isinflated and/or deflated using a second port 9204B coupled to the secondinflatable portion 9202B via a tube 9206B. The tube 9206B and inflatableportion 9202B are positioned within a chamber 9210B formed in thepolymer material of the clamp 9200 and are coupled together at aninterface 9208B. In its inflated state, the second inflatable portion9202B generally fills the chamber 9210B and takes the shape of the rigidsubstrate member 4103 (see FIG. 41(a)) and functions in a manner similarto the substrate member 4103 as discussed above. When deflated, thesecond inflatable portion 9202B is positioned within the chamber 9210Bin a flaccid state.

In the embodiment shown in FIG. 92, the port 9204A is positioned on afirst arm 9212 of the clamp 9200. The first arm 9212 is formed of apolymer material having the chamber 9210A formed therein to house thefirst inflatable portion 9202A and first tube 9206A. The first arm 9212forms the first elongated portion 9214 of the clamp 9200, a portion ofthe bight portion 9218 of the clamp 9200, and the engagement portion9224. Although the port 9204A is shown on the first arm 9212 of theclamp 9200, the port 9204A may be placed in other locations including,for example, the bight portion 9218 of the clamp 9200.

Similarly, the port 9204B is positioned on a second arm 9226 of theclamp 9200. The second arm 9226 is formed of a polymer material havingthe chamber 9210B formed therein to house the second inflatable portion9202B and second tube 9206B. The second arm 9226 forms the secondelongated portion 9216 of the clamp 9200, a portion of the bight portion9218 of the clamp 9200, and the fastener portion 9222. Although the port9204B is shown on the second arm 9226 of the clamp 9200, the port 9204Bmay be placed in other locations including, for example, the bightportion 9218 of the clamp 9200.

Additionally, in accordance with other embodiments disclosed herein, thefirst and second inflatable portions 9202 may share a single port 9204located anywhere on the clamp 9200. An example of such an embodiment isillustrated in FIG. 93, wherein the clamp 9300 has a port 9304 locatedon the flexible hinge 9320 of the bight portion 9318. The clamp 9300 isidentical to the clamp 9200 of FIG. 92 except that the clamp 9300 hasone port 9304 connected to both a first tube 9306A and a second tube9306B. The first tube 9306A connects to the first inflatable portion9302A at an interface 9308A. The first inflatable portion 9302A ispositioned within a chamber 9310A in a first arm 9312 of the clamp 9300.The second tube 9306B connects to the second inflatable portion 9302B atan interface 9308B. The second inflatable portion 9302B is positionedwithin a chamber 9310B in a second arm 9326 of the clamp 9300. In otherembodiments, the port(s) 9204 or 9304 may be a subcutaneous port. Itshould be understood that other embodiments may be provided such as, forexample, one or more subcutaneous ports each designated for eachinflatable portion, and a single port connected to one or more of theinflatable portions via one or more tubes.

In some embodiments, a clamp may include inflatable portions atdifferent locations within the clamp. For example, FIG. 94 illustratesan embodiment of a clamp 9400 having a first set of inflatable portions9402A and 9402B located in the bight portion 9418 of the clamp 9400, anda second set of inflatable portions 9404A and 9404B located inrespective elongated portions 9414 and 9416 of the clamp 9400. The clamp9400 includes a first arm 9412 and a second arm 9426 and operatessimilar to clamps 9200 and 9300.

The first set of inflatable portions 9402A and 9402B are inflated and/ordeflated using a port 9405 located on the bight portion 9418. The port9405 is connected to both a first tube 9403A and a second tube 9403B.The first tube 9403A connects to the first inflatable portion 9402A atan interface 9408A. The first inflatable portion 9402A and first tube9403A are positioned within a chamber 9410A in the bight portion 9418 ofthe clamp 9400. The second tube 9403B connects to the second inflatableportion 9402B at an interface 9408B. The second inflatable portion 9402Band second tube 9403B are positioned within a chamber 9410B in the bightportion 9418 of the clamp 9400.

The second set of inflatable portions 9404A and 9404B are inflatedand/or deflated using respective ports 9415A and 9415B located on therespective first and second arms 9412 and 9426 of the clamp 9400. Theport 9415A is connected to a first tube 9413A. The first tube 9413Aconnects to the first inflatable portion 9404A at an interface 9409A.The first inflatable portion 9404A and the first tube 9413A arepositioned within a chamber 9411A in the first arm 9412 of the clamp9400. The port 9415B is connected to a second tube 9413B. The secondtube 9413B connects to the second inflatable portion 9404B at aninterface 9409B. The second inflatable portion 9404B and the second tube9413B are positioned within a chamber 9411B in the second arm 9426 ofthe clamp 9400.

The clamp 9400 is similar to clamps 9200 and 9300 except that theinflatable substrate members are divided into multiple portions.Specifically, the first set of inflatable portions 9402 is located inthe bight portion 9418 and the second set of inflatable portions 9404 islocated in the elongated portions 9414 and 9416 of the clamp 9400. Thefirst set of inflatable portions 9402 may be inflated/deflatedseparately from the second set of inflatable portions 9404 using theport 9405 located in the bight portion 9418 of the clamp 9400. Thesecond set of inflatable portions 9404 may be inflated/deflated viaports 9415A and 9415B located on the first arm 9412 and second arm 9426,respectively, of the clamp 9400. Thus, the air pressure of therespective first and second sets of inflatable portions 9402 and 9404may be controlled and/or adjusted independently. Specifically, the firstset of inflatable portions 9402 may be controlled and/or adjustedindependently from the second set of inflatable portions 9404.Additionally, the first inflatable portion 9404A of the second set maybe controlled and/or adjusted separately from the second inflatableportion 9404B of the second set. This is because a different port isused to control and/or adjust the inflation/deflation of each respectiveinflatable portion. Although it is not illustrated, in some embodiments,a separate port may be used to independently control and/or adjust eachof the first and second inflatable portions 9402A and 9402B comprisingthe first set of inflatable portions. In other words, a first port couldbe used to control and/or adjust the air pressure of the firstinflatable portion 9402A and a second port could be used to controland/or adjust the air pressure of the second inflatable portion 9402B.

Referring again to FIG. 92, the clamp 9200 and portions of the clamp9200, and other similar clamps and similar portions of those clamps, maybe used as discussed herein in accordance with the foregoing disclosure(e.g., to partition the stomach, to allow flexing with the flexiblehinge 9220, to be installed via trocar, to be installed in anexpanded/open position, to retain the clamp 9200 in a closed position,etc.), but with the added benefits provided by the inflatable portions9202. For example, the first and second elongated portions 9214 and 9216generally form a partition-forming section of the clamp 9200, and thebight portion 9218 generally forms a passage-forming section of theclamp 9200, as should be understood from the foregoing disclosure. Thepartition-forming and passage-forming sections (and the clamp 9200, ingeneral) operate in accordance with the disclosure provided for otherclamp embodiments discussed herein, but with the added benefits providedby the inflatable portions 9202.

One benefit of using inflatable portions 9202 in lieu of the substratemembers is that the clamp 9200 is more flexible, especially when theinflatable portions 9202 are deflated, thereby allowing for easierinstallation. For example, when the inflatable portions 9202 aredeflated, the clamp 9200 is more flexible, and may be inserted into atrocar more easily and may be more easily manipulated when installingthe clamp 9200 on a patient's stomach. What's more, the inflatableportions 9202 become more rigid as they are inflated. Therefore, one ormore of the inflatable portions 9202 may be inflated as desired when itis preferable to have respective arms of the clamp 9202 in a rigidstate. Conversely, one or more of the inflatable portions 9202 may bedeflated as desired when it is preferable to have respective arms of theclamp 9202 in a more flexible state.

Additionally, the inflatable portions 9202 may, in some embodiments, beadjusted by inflating or deflating the respective inflatable portions9202 such that a desired rigidity of the inflatable portions 9202 isachieved. This allows for the clamp 9202 to provide a customized andadjustable fit and/or pressure applied to the patient's stomach, whichmay be adjusted as desired. In some embodiments, the inflatable portions9202 are not adjustable.

As previously mentioned, the inflatable portions may be used assubstitutes for the rigid substrate members of any of the clampembodiments disclosed herein. For example, FIGS. 95(a) and 95(b)illustrate example embodiments of a clamp 9500 similar to the angledclamp embodiment described above with respect to FIGS. 54(a) and 54(b),wherein the clamp 9500 includes inflatable substrates as substitutes forthe rigid substrate members 4301, 4303, and 4307 described in connectionwith FIGS. 54(a) and 54(b). The clamp 9500 operates similar to the clamp4300 described in FIGS. 54(a) and 54(b), except that the rigid substratemembers are replaced with inflatable substrate members.

Specifically, in FIGS. 95(a) and 95(b) the clamp 9500 is installed on astomach 9550 and includes a first inflatable substrate 9502 comprisingat least a portion of the first elongated portion 9504, a secondinflatable substrate 9506 comprising at least a portion of the bightportion 9508, and a third inflatable substrate (not shown) comprising atleast a portion of a second elongated portion (not shown) positioned onan opposite side of the stomach 9550 from the first elongated portion9504. As shown in FIG. 95(a), one or more adjustable portions 9510 arehinged such that the bight portion 9508 is angled in a first directionrelative to the first elongated portion 9504 and second elongatedportion. As shown in FIG. 95(b), one or more adjustable portions 9510are hinged such that the bight portion 9508 is angled in a seconddirection relative to the first elongated portion 9504 and secondelongated portion. It should understood that the ports and tubes are notshown in FIGS. 95(a) and 95(b). Additionally, the bight portion mayinclude only one inflatable substrate, or may include two or moreinflatable substrates.

With reference to FIG. 96, a bariatric clamp 9600 is disclosed.Bariatric clamp 9600 may comprise aspects of any one of the bariatricclamps discussed herein above and/or may comprise combinations ofaspects of bariatric clamps discussed herein above in addition tofurther features. For example, bariatric clamp 9600 may comprise a tipstring 9603 configured to aid installation of the bariatric clamp 9600.In various embodiments, tip string 9603 comprises a suture thread,although in further instances, a polymeric extension, or an embeddedflexible member, and/or any aspect extending flexibly from a tip of aportion 9601 of the bariatric clamp 9600 and capable of being grasped bya tool during installation of the bariatric clamp 9600 may be used. Invarious embodiments, tip string 9603 comprises a suture thread installedinto the bariatric clamp 9600 by a needle and tied around an aspect ofthe bariatric clamp 9600 such as an internal structure and/or anovermold of the bariatric clamp 9600. In further instances, tip string9603 comprises a suture thread formed into the bariatric clamp 9600during initial construction, such as extending from an internalstructure of the bariatric clamp 9600 and outwardly through an overmoldaspect of the bariatric clamp 9600. In various instances, the tip string9603 may be configured to be grasped by a tool during installation ofthe bariatric clamp 9600 to position the bariatric clamp 9600 and/or toaid closure of the bariatric clamp 9600. Moreover, while the tip string9603 is depicted at the distal end of a portion 9601 of the bariatricclamp 9600, one may appreciate that the tip string 9603 may attach atother positions, including midpoints of portions of the bariatric clamp9600. A tip string 9603 may have a length sufficient to facilitategrasping and use to aid installation of the bariatric clamp. Thus thelength of a tip string 9603 may in different embodiments be differentlengths depending on the position at which the tip string 9603 isattached.

Embodiments of the foregoing clamps having inflatable portions may beinstalled in accordance with the installation procedures provided hereinfor the various clamp embodiments. For example, the clamps 8500 and 9200are similar to the clamp 4100 provided in FIGS. 41(a)-41(e) anddiscussed herein. As such, the clamps 8500 and 9200 may be installed inaccordance with the disclosed installation methods for the clamp 4100(and other similar clamps). These clamps, as well as other clampembodiments disclosed herein, may be installed using an insertion orinstallation tool, or may be installed without use of such tool.Additionally, the clamp 9100 is similar to the clamp 7000 provided inFIG. 70 and discussed herein as having various suture portions. As such,the clamp 9100 may be installed in accordance with the disclosedinstallation methods for the clamp 7000 (and other similar clamps).Again, this clamp, and other clamp embodiments disclosed herein, may beinstalled using an insertion or installation tool, or may be installedwithout use of such tool. Moreover, according to FIG. 96 each embodimentof the foregoing clamps may include a tip string 9603 similar tobariatric clamp 9600 in addition to their own distinctive features andeach installation method may make use of a tip string 9603.

In the installation procedures provided herein, care should be taken toavoid puncturing the inflatable portions. In the embodiments disclosedherein, the inflatable portions may be formed of any material that iscapable of achieving the desired effects described herein. In someembodiments, the inflatable portions and/or chambers in which theinflatable portions are positioned may include a lining, coating, orbarrier that protects the inflatable portions from punctures,particularly from needles used to suture the clamp.

It should be appreciated that various modifications may be made to thedisclosed clamp without departing from the scope of the presentdisclosure. For example, in some embodiments, the inflatable portionsmay extend beyond the partition-forming section, or may otherwise bepositioned along the bight or flexible hinge portions of the clamp. Insome embodiments, the inflatable portions may be provided to adjust thesize of the passage formed by the passage-forming section of the clamp.In such embodiments, the inflatable portions may be provided solely onthe passage-forming section of the clamp, or may alternately be providedto extend along both the partition-forming and passage-forming sectionsof the clamp. In embodiments providing inflatable portions to adjust thepassage, the inflatable portions may be provided in the clamp in amanner similar to the various embodiments disclosed herein (e.g.,embedded within the polymer overmolding and within a substrate member,on a surface of the polymer overmolding, and between the polymerovermolding and substrate member). Additionally, the pressure ofinflatable portions may be adjusted via ports and tubes as discussed inthe various embodiments provided herein.

A number of additional and alternative embodiments of the surgicalclamps, installation tools and methods for installing can havecharacteristics that are different from those described above. Forexample, it is envisioned that a surgical clamp not intended forbariatric surgery might not have a passage forming section, and thatsuch a clamp might be smaller or larger, depending on the purpose of theclamp. For example, the clamp can be one-tenth of an inch in length topartition a blood vessel, or twenty-two centimeters in length topartition a stomach. Moreover, the clamp can be configured to partitionany internal organ, and can vary in length accordingly between these twoexample lengths, or be longer or shorter as required. Also, the guidemembers might have one or more protrusions aligned with the engagementfeature and configured for insertion into the slot formed in the bightportion of the clamp. Moreover, it is envisioned that the installationtool can be integrated with an endoscope and/or surgical robot, and thatappropriate robotic elements can be included in place of or in additionto those described above. These and other features can be included invarious combinations without departing from the scope of the inventionas defined in the following aspects.

The invention claimed is:
 1. A bariatric clamp comprising: a firstelongated portion having (i) a portion of a first substrate member and(ii) a first polymer portion; a second elongated portion having (i) aportion of a second substrate member and (ii) a second polymer portion,wherein each of the first substrate member and the second substratemember is bent; wherein the bend in each of the first substrate memberand the second substrate member is away from the other of the firstsubstrate member and the second substrate member, such that the bendsincrease a spacing between the first substrate member and the secondsubstrate member, a bight portion having a flexible hinge formed atleast partially from a third polymer portion joining the first substratemember and the second substrate member; a first inflatable portiondisposed at least partially within a first recess in the first substratemember and positioned between a surface of the first substrate memberand an interior surface of the first polymer portion of the firstelongated portion of the bariatric clamp; a second inflatable portiondisposed at least partially within a second recess in the secondsubstrate member and positioned between a surface of the secondsubstrate member and an interior surface of the second polymer portionof the second elongated portion of the bariatric clamp; and a portcoupled to at least one of the first and second inflatable portions andconfigured to adjust inflation of the one or more of the first andsecond inflatable portions.
 2. The bariatric clamp of claim 1, whereinthe port is disposed on the first elongated portion and is coupled tothe first inflatable portion via a tube that is disposed along aninterior chamber of the first elongated portion and is connected to thefirst inflatable portion at an interface positioned adjacent the firstelongated portion and the first inflatable portion.
 3. The bariatricclamp of claim 2, further comprising a second port coupled to the secondinflatable portion and configured to adjust inflation of the secondinflatable portion.
 4. The bariatric clamp of claim 1, wherein the portis a subcutaneous port, and is connected to at least one of the firstinflatable portion and the second inflatable portion via a tube.
 5. Thebariatric clamp of claim 1, wherein the port is disposed on the firstelongated portion and is coupled to the first inflatable portion via afirst tube, and is coupled to the second inflatable portion via a secondtube.
 6. The bariatric clamp of claim 1, wherein the port is disposed onthe bight portion and coupled to the first inflatable portion via afirst tube, and is coupled to the second inflatable portion via a secondtube.
 7. The bariatric clamp of claim 1, wherein the second inflatableportion is at least partially disposed on at least a portion of thebight portion.
 8. The bariatric clamp of claim 1, wherein a spacingbetween the first elongated portion and the second elongated portion isadjustable by inflating at least one of the first inflatable portion andthe second inflatable portion.
 9. The bariatric clamp of claim 1,wherein the first and second elongated portions of the bariatric clampform a partition-forming section located towards a first end of thebariatric clamp when the bariatric clamp is in a substantially closedposition, and the bight portion of the bariatric clamp forms apassage-forming section located towards a second end of the bariatricclamp when the bariatric clamp is in the substantially closed position.10. The bariatric clamp of claim 1, wherein at least one of the firstinflatable portion and the second inflatable portion are configured toinflate or deflate to adjust a pressure applied by the partition-formingsection of the clamp.
 11. The bariatric clamp of claim 1, furthercomprising: a fastener portion disposed on the second elongated portion;and an engagement portion disposed on the first elongated portion, theengagement portion operable to engage the fastener portion to retain thebariatric clamp in a substantially closed position.
 12. A bariatricclamp comprising: a first elongated portion having (i) at least aportion of a first substrate member, and (ii) a first polymer portion; asecond elongated portion having (i) at least a portion of a secondsubstrate member, and (ii) a second polymer portion; wherein at leastone of the first substrate member and the second substrate memberincludes a bend, a bight portion having a flexible hinge formed at leastpartially from a third polymer portion, and the bight portion positionedbetween the first elongated portion and the second elongated portion;wherein the bend in at least one of the first substrate member and thesecond substrate member is away from the other of the first substratemember and the second substrate member, such that the bend increases aspacing between the first substrate member and the second substratemember, a first inflatable portion disposed between a surface of thefirst substrate member and an interior surface of the first polymerportion of the first elongated portion of the bariatric clamp; a secondinflatable portion disposed between a surface of the second substratemember and an interior surface of the second polymer portion of thesecond elongated portion of the bariatric clamp; and a port coupled toat least one of the first inflatable portion and the second inflatableportion, and the port configured to adjust inflation of the one or moreof the first inflatable portion and the second inflatable portion. 13.The bariatric clamp of claim 12, wherein the bend is provided in thefirst substrate member and is bent away from the second substratemember, such that the bend increases a spacing between the firstsubstrate member and the second substrate member.
 14. The bariatricclamp of claim 13, wherein a second bend is provided in the secondsubstrate member and is bent away from the first substrate member, suchthat the second bend increases the spacing between the first substratemember and the second substrate member.
 15. The bariatric clamp of claim14, wherein the bend in the first substrate member and the second bendin the second substrate member are in opposite directions away from eachother.
 16. The bariatric clamp of claim 12, wherein the port is disposedon the first elongated portion and coupled to the first inflatableportion via a tube that is disposed along an interior chamber of thefirst elongated portion and is connected to the first inflatable portionat an interface positioned adjacent the first elongated portion and thefirst inflatable portion.
 17. The bariatric clamp of claim 12, whereinthe port is coupled to the first inflatable portion and is configured toadjust inflation of the first inflatable portion, and further comprisinga second port coupled to the second inflatable portion and configured toadjust inflation of the second inflatable portion.
 18. The bariatricclamp of claim 12, wherein the port is a subcutaneous port, and isconnected to the first inflatable portion via a tube.
 19. The bariatricclamp of claim 12, wherein the port is disposed on the first elongatedportion and is coupled to the first inflatable portion via a first tube,and is coupled to the second inflatable portion via a second tube. 20.The bariatric clamp of claim 12, wherein the port is disposed on thebight portion and coupled to the first inflatable portion via a firsttube, and is coupled to the second inflatable portion via a second tube.21. The bariatric clamp of claim 12, wherein the second inflatableportion is at least partially disposed on at least a portion of thebight portion.
 22. The bariatric clamp of claim 12, wherein a spacingbetween the first elongated portion and the second elongated portion isadjustable by inflating at least one of the first inflatable portion andthe second inflatable portion.
 23. The bariatric clamp of claim 12,wherein the first elongated portion and second elongated portion of thebariatric clamp form a partition-forming section located towards a firstend of the bariatric clamp when the bariatric clamp is in asubstantially closed position, and the bight portion of the bariatricclamp forms a passage-forming section located towards a second end ofthe bariatric clamp when the bariatric clamp is in the substantiallyclosed position.
 24. The bariatric clamp of claim 12, wherein at leastone of the first inflatable portion and the second inflatable portionare configured to inflate or deflate to adjust a pressure applied by thepartition-forming section of the clamp.
 25. The bariatric clamp of claim12, further comprising: a fastener portion disposed on the secondelongated portion; and an engagement portion disposed on the firstelongated portion, the engagement portion operable to engage thefastener portion to retain the bariatric clamp in a substantially closedposition.
 26. The bariatric clamp of claim 12, wherein the first polymerportion, the second polymer portion, and the third polymer portion areprovided as a single polymer portion.